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1.
J Cell Mol Med ; 28(7): e18181, 2024 04.
Artigo em Inglês | MEDLINE | ID: mdl-38506077

RESUMO

This study aimed to analyse the association between sex hormones and bone age (BA) in boys aged 9-18 years, both individually and interactively, and further to explore whether nutritional status may influence this association. A retrospective analysis was performed among 1382 Chinese boys with physical measurements, sexual characteristics, BA radiographs and sex hormone indicators from February 2015 to February 2022. A total of 470 (34.0%) boys had advanced BA. BA was positively associated with estradiol, luteinizing hormone (LH), follicle-stimulating hormone (FSH) and testosterone in both advanced and normal BA groups after adjusting for age, genetic height and body mass index. Multiple logistic regression showed that after adjusting for covariates, estradiol (odds ratio [OR] = 1.66, 95% confidence interval [CI]: 1.14-2.12), LH (OR = 1.43, 95% CI: 1.04-1.96), and testosterone (OR = 1.58, 95% CI: 1.17-2.13) were significantly associated with the increased risk of advanced BA in boys, and the association was reinforced when these hormones were interactively explored. Stratified by nutritional status, the interaction between estradiol, LH, and testosterone showed a strong association with advanced BA in boys with normal weight.


Assuntos
Hormônios Esteroides Gonadais , Hormônio Luteinizante , Masculino , Humanos , Feminino , Estudos Retrospectivos , Testosterona , Estradiol
2.
J Exp Child Psychol ; 239: 105826, 2024 03.
Artigo em Inglês | MEDLINE | ID: mdl-38118379

RESUMO

Imitation that entails faithful reproduction of demonstrated behavior by reenacting a sequence of actions accurately is a fast and efficient way to acquire new skills as well as to conform to social norms. Previous studies reported that both culture and gender might impinge on young children's fidelity of imitation. We analyzed the imitative behavior of 87 children whose ages ranged from 3 to 6 years. An instrumental task was administered that offered partial (opaque apparatus) or total (transparent apparatus) information about causal connection between the demonstrated actions and their effect in achieving a desired reward. Imitative fidelity (imitating the actions that were demonstrated by an adult model yet were unnecessary for achieving the instrumental goal) increased as a function of age in boys, whereas no differences were found in girls. This lack of increase in girls can be ascribed to their displaying higher degrees of imitation fidelity at an earlier age.


Assuntos
Comportamento Imitativo , Motivação , Masculino , Criança , Feminino , Humanos , Pré-Escolar , Normas Sociais
3.
Wiad Lek ; 77(1): 171-177, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38431823

RESUMO

We reported the case of tonsillitis treatment in a 17-years-old boy with use of chemical non-antibiotic preparations, plant derived products and antibiotic benzathine phenoxymethylpenicillin. The antimicrobial agents for treatment were selected on the basis of their activity against a disease agent, the group A ß-hemolytic strain Streptococcus pyogenes BS1 isolated from a patient. The bacterium was susceptible in vitro to ß-lactams, with largest zones conditioned by penicillin G and benzathine phenoxymethylpenicillin discs, to fluoroquinolones and to cephems, with exception of cefazolin. Lincosamide clindamycin, macrolide spiramycin, aminoglycoside gentamicin, erythromycin, tetracycline and combination of sulfamethoxazole and trimethoprim were inactive against this bacterium. The Streptococcus pyogenes BS1 demonstrated intermediate susceptibility to the cephalosporin cephalexin, fluoroquinolone lomefloxacin and glycopeptide vancomycin. Non-antibiotic preparations were evaluated against Streptococcus pyogenes BS1 also. Among them "Stomatidin", "Chlorophyllipt", and phages of "Pyofag" were more effective than "Decatylen", "Decasan" and "Furadonin" in vitro. The antimicrobial applications of "Stomatidin", "Chlorophyllipt" and phages of "Pyofag" in the patient were less effective compared to the result of antibiotic benzathine phenoxymethylpenicillin treatment. Complete recovery of the patient was achieved with use of this antibiotic and Calendula flower extract as an local anti-inflammatory agent.


Assuntos
Anti-Infecciosos , Etilenodiaminas , Tonsilite , Adolescente , Humanos , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Penicilina V/farmacologia , Streptococcus pyogenes , Tonsilite/tratamento farmacológico
4.
J Clin Lab Anal ; 36(1): e24123, 2022 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34791706

RESUMO

BACKGROUND: Variants in the endosomal solute carrier family 9 member A6 (SLC9A6)/(Na+ ,K+ )/H+ exchanger 6 (NHE6) gene have been linked to epilepsy, speech loss, truncal ataxia, hyperkinesia, and postnatal microcephaly. METHODS: In the present study, we evaluated genetic alterations in a 3-year-old Chinese boy displayed features of epilepsy, psychomotor retardation, microcephaly, low body weight, difficulty in feeding, excessive movement, attention loss, ataxia, and cerebellar atrophy and his healthy family using WES method. The identified variant was further confirmed by Sanger sequencing method. Finally, minigene assays were used to verify whether the novel SLC9A6 intronic variant influenced the normal splicing of mRNA. RESULTS: We identified a novel hemizygous splicing variant [NM_001042537.1: c.1463-1G>A] in SLC9A6 by trio-based exome sequencing. The minigene expression in vitro confirmed the splicing variant altered a consensus splice acceptor site of SLC9A6 intron 11, resulting in skipping over exon 12. CONCLUSIONS: Our finding extends the catalog of pathogenic intronic variants affecting SLC9A6 pre-mRNA splicing and provides a basis for the genetic diagnosis of CS.


Assuntos
Ataxia/genética , Epilepsia/genética , Doenças Genéticas Ligadas ao Cromossomo X/genética , Deficiência Intelectual/genética , Microcefalia/genética , Transtornos da Motilidade Ocular/genética , Trocadores de Sódio-Hidrogênio/genética , Pré-Escolar , China , Humanos , Masculino , Isoformas de Proteínas/genética , Sequenciamento do Exoma
5.
Mol Biol Rep ; 47(10): 7623-7632, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32996047

RESUMO

Autism is heterogeneous multifactorial neurodevelopmental and neuropsychiatric disorder with repetitive and limited behaviors as well as communication deficits. Prevalence of autism in males is predominant than females, but their genetic association is unclear. The study was performed to investigate Y-chromosome haplotypes, significant risk variants and susceptibility genes associated with autistic Saudi young males with autism. Exome genotyping microarray analysis was performed in Saudi young boys with autism (cases, n = 47) and without autism and other genetic or neurodevelopmental disorders (control, n = 43) to identify the functional exonic risk variations among 243,345 exonic variations. The most significant single nucleotide polymorphisms (SNPs) of protein coding associated with autism in Saudi young boys were studied for functional enrichment. Y-chromosome haplotyping analysis of 6 SNPs such as rs1865680, rs2032624, rs2032658, rs2032631, rs9786153 and rs13447352 uncovered the most significant protective (ACGACA p = 2.94 × 10-9) among the controls and the high risk Y-haplotype (GAAGTC p = 6.85 × 10-6) among autistic boys. Exome association study revealed 6 susceptible genes, MCC, AUTS2, VSX1, SETBP1, CNTN3, and PCDH11Y that were known for autistic disorder. The significant predisposed genes with functional variants of Y-chromomere are strongly connected with spermatogenic failure (p = 8.02 × 10-8), azoospermia (p = 6.32 × 10-7), partial chromosome Y deletion (p = 7.66 × 10-6), HDMs demethylate histones pathway (p = 3.55 × 10-4) and immune system diseases (p = 4.11 × 10-3). Y-haplotypes and highly significant pathogenic exonic variants in MCC, AUTS2, VSX1, SETBP1, CNTN3 and PCDH11Y genes are more influential genetic factors for developing autism in boys of Arab origin.


Assuntos
Árabes/genética , Transtorno Autístico/genética , Cromossomos Humanos Y/genética , Predisposição Genética para Doença , Haplótipos , Polimorfismo de Nucleotídeo Único , Criança , Pré-Escolar , Estudo de Associação Genômica Ampla , Humanos , Masculino , Projetos Piloto , Fatores de Risco , Sequenciamento do Exoma
6.
Res Sports Med ; 28(4): 507-517, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32573266

RESUMO

Participation and performance trends as well as the performance differences among sexes in ultra-endurance running have been well described in the adult population; however, less information on such trends existed in youth ultramarathoners. The aim of the present study was to investigate the age-related participation and performance trends of children and adolescent ultramarathoner runners. Data on runners, younger than 19 years of age, competing from 1960 to 2018 in distance-limited ultramarathons of 50 km, 100 km, 50 miles and 100 miles, were analysed. During this period, the number of ultramarathon participation increased, most notably among boys, most runners originated from Europe, and the 50- and 100-km race distances were the most popular. Overall, male runners were faster than female runners, except in the case of European and Oceanian origin, where girls were faster over the 50-km race. The fastest male runners originated from Africa and the fastest girls from Oceania, and the average running speed has largely decreased for both sexes over calendar years. In summary, this study was the first to report details on participation and performance trends in youth ultramarathoners competing in distance-limited ultramarathons.


Assuntos
Desempenho Atlético/tendências , Corrida de Maratona/tendências , Adolescente , África , Fatores Etários , Ásia , Criança , Europa (Continente) , Feminino , Humanos , Masculino , América do Norte , Oceania , Fatores Sexuais
7.
Am J Kidney Dis ; 73(2): 156-162, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30318132

RESUMO

RATIONALE & OBJECTIVE: In the general population, girls have lower mortality risk compared with boys. However, few studies have focused on sex differences in survival and in access to kidney transplantation among children with end-stage kidney disease. STUDY DESIGN: Retrospective cohort study. SETTING & PARTICIPANTS: Children aged 2 to 19 years registered in the US Renal Data System who started renal replacement therapy (RRT) between 1995 and 2011. PREDICTOR: Study participant sex. OUTCOME: Time to death and time to kidney transplantation. ANALYTICAL APPROACH: We used adjusted Cox models to examine the association between sex and all-cause mortality. We used Fine-Gray models to examine the association between sex and kidney transplantation accounting for the competing risk for death. RESULTS: We included 14,024 children, of whom 1,880 died during a median 7.1 years of follow-up. In adjusted analyses, the HR for death was higher for girls (HR, 1.36; 95% CI, 1.25-1.50) than boys. When we further adjusted our survival models for transplantation as a time-dependent covariate, the hazard rate of death in girls was partially attenuated but remained statistically significantly higher than that for boys (HR, 1.28; 95% CI, 1.17-1.41). Girls were also less likely to receive a kidney transplant than boys (adjusted subdistribution HR, 0.91; 95% CI, 0.88-0.95) in analyses treating death as a competing risk. LIMITATIONS: Lack of data for disease course before the onset of RRT and observational study data. CONCLUSIONS: The mortality rate was substantially higher for girls than for boys treated with RRT. Access to transplantation was lower for girls than boys, but differences in transplantation access accounted for only a small proportion of the survival differences by sex.


Assuntos
Causas de Morte , Disparidades nos Níveis de Saúde , Falência Renal Crônica/diagnóstico , Falência Renal Crônica/mortalidade , Adolescente , Fatores Etários , Criança , Pré-Escolar , Estudos de Coortes , Feminino , Humanos , Falência Renal Crônica/terapia , Transplante de Rim/métodos , Transplante de Rim/mortalidade , Masculino , Modelos de Riscos Proporcionais , Sistema de Registros , Diálise Renal/métodos , Diálise Renal/mortalidade , Estudos Retrospectivos , Medição de Risco , Índice de Gravidade de Doença , Fatores Sexuais , Análise de Sobrevida , Estados Unidos
8.
Clin Endocrinol (Oxf) ; 90(5): 702-710, 2019 05.
Artigo em Inglês | MEDLINE | ID: mdl-30739355

RESUMO

OBJECTIVE: We examined the associations between maternal age at menarche and anthropometry and metabolism in adolescent offspring. METHODS: Anthropometric, metabolic and blood pressure data were obtained from 304 girls and 190 boys aged 11-16 years attending school in Hangzhou (China). Age at menarche for both mothers and daughters was self-reported. Fasting blood samples were obtained and all participants underwent clinical examinations. Obesity was defined as BMI ≥95th percentile for age and sex. RESULTS: Older maternal age at menarche was associated with older age of their daughters at menarche (r = 0.21; P < 0.001). Mother's age at menarche was not associated with anthropometry or metabolism of daughters. However, younger maternal age at menarche was associated with increased hip and waist circumferences, and BMI SDS of their sons. Boys whose mothers were ≤13 years at menarche had an adjusted relative risk of obesity 3-fold greater than sons of mothers with a later menarcheal onset (2.96; 95% CI 1.49, 5.87). Among daughters, every 1-year increase in their age at menarche was associated with a 0.34 SDS reduction in BMI. Increasing age at menarche was also associated with reduced waist and hip circumferences (-1.5 and -1.8 cm/y, respectively) and waist-to-height ratio (-0.008 per year). Girls in the youngest menarcheal age tertile (8.8-11.6 years) had diastolic blood pressure 2.2 mm Hg higher than other girls (P = 0.029). CONCLUSIONS: Younger maternal age at menarche is associated with increased obesity risk in their sons, but not daughters. However, girls who experience menarche earlier have a less favourable anthropometric profile.


Assuntos
Pressão Sanguínea , Índice de Massa Corporal , Menarca , Mães/estatística & dados numéricos , Obesidade Infantil/epidemiologia , Caracteres Sexuais , Circunferência da Cintura , Razão Cintura-Estatura , Adolescente , Fatores Etários , Pressão Sanguínea/fisiologia , Criança , China/epidemiologia , Feminino , Humanos , Masculino , Menarca/fisiologia , Risco , Circunferência da Cintura/fisiologia
9.
Neuroophthalmology ; 43(2): 114-119, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-31312236

RESUMO

Ophthalmic and MRI evaluations of a 13-year-old boy who reported loss of visual acuity in his right eye demonstrated the presence of unilateral optic neuritis. After serological tests showed positivity for anti-aquaporin 4 antibody, he was diagnosed with neuromyelitis optica spectrum disorder. Encephalopathy and myelitis were not observed. Since his unilateral optic neuritis was considered to reflect mild disease activity, only follow-up observations were performed. Visual acuity and central scotoma improved 1 week after the first examination. In the absence of any specific treatments, good visual acuity has remained for 20 months, with no relapse of optic neuritis.

10.
J Magn Reson Imaging ; 2018 Feb 13.
Artigo em Inglês | MEDLINE | ID: mdl-29437252

RESUMO

BACKGROUND: Subject motion is known to produce spurious covariance among time-series in functional connectivity that has been reported to induce distance-dependent spurious correlations. PURPOSE: To present a feasibility study for applying the extended Kalman filter (EKF) framework for high temporal resolution motion correction of resting state functional MRI (rs-fMRI) series using each simultaneous multi-slice (SMS) echo planar imaging (EPI) shot as its own navigator. STUDY TYPE: Prospective feasibility study. POPULATION/SUBJECTS: Three human volunteers. FIELD STRENGTH/SEQUENCE: 3T GE DISCOVERY MR750 scanner using a 32-channel head coil. Simultaneous multi-slice rs-fMRI sequence with repetition time (TR)/echo time (TE) = 800/30 ms, and SMS factor 6. ASSESSMENT: Motion estimates were computed using two techniques: a conventional rigid-body volume-wise registration; and a high-temporal resolution motion estimation rigid-body approach. The reference image was resampled using the estimates obtained from both approaches and the difference between these predicted volumes and the original moving series was summarized using the normalized mean squared error (NMSE). STATISTICAL TESTS: Direct comparison of NMSE values. RESULTS: High-temporal motion estimation was always superior to volume-wise motion estimation for the sample presented. For staged continuous rotations, the NMSE using high-temporal resolution motion estimates ranged between [0.130, 0.150] for the first volunteer (in-plane rotations), between [0.060, 0.068] for the second volunteer (in-plane rotations), and between [0.063, 0.080] for the third volunteer (through-plane rotations). These values went up to [0.384, 0.464]; [0.136, 0.179]; and [0.080, 0.096], respectively, when using volume-wise motion estimates. DATA CONCLUSION: Accurate high-temporal rigid-body motion estimates can be obtained for rs-fMRI taking advantage of simultaneous multi-slice EPI sub-TR shots. LEVEL OF EVIDENCE: 2 Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2018.

11.
Cardiol Young ; 28(10): 1165-1167, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-30047352

RESUMO

Kounis Syndrome is characterised by the concurrence of acute coronary syndrome with mast cell activation induced by inflammatory mediators released during an allergic reaction. Although several factors and diseases were reported to be associated with Kounis Syndrome, branched-chain amino acid supplements have not been previously reported as a cause of Kounis Syndrome. We present a 17-year-old boy admitted to our hospital with thoracic pain after the ingestion of a branched-chain amino acid supplement.


Assuntos
Aminoácidos de Cadeia Ramificada/efeitos adversos , Eletrocardiografia , Hipersensibilidade/etiologia , Síndrome de Kounis/etiologia , Adolescente , Angiografia Coronária , Diagnóstico Diferencial , Suplementos Nutricionais/efeitos adversos , Ecocardiografia , Humanos , Hipersensibilidade/diagnóstico , Síndrome de Kounis/diagnóstico , Masculino
12.
Acta Medica (Hradec Kralove) ; 61(2): 41-46, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30216181

RESUMO

The aim of this study is to describe an entity of primary hydrocele accompanied with fibrosis, thickening and hemorrhagic infiltration of parietal layer of tunica vaginalis (PLTV). During a 4-year period (2011-2014), 94 boys (2.5-14 years old) underwent primary hydrocele repair. Hydrocele was right sided in 55 (58.5 %), left sided in 26 (28.7%) and bilateral in 12 patients (13.8%). Eighty three out of 94 patients (88.30%) had communicating hydrocele and the rest eleven patients (11.7%) had non-communicating. Our case group consists of 8 patients (8.51%) based on operative findings consistent with PLTV induration, thickening and hemorrhagic infiltration. Preoperative ultrasonography did not reveal any pathology of the intrascrotal structures besides hydrocele. There weren't hyperechoic reflections or septa within the fluid. Evaluation of thickness of the PLTV was not feasible. Presence of lymph or exudate was excluded after fluid biochemical analysis. Tunica vaginalis histological examination confirmed thickening, hemorrhagic infiltration and inflammation, while there was absence of mesothelial cells. Immunochemistry for desmin was positive, excluding malignant mesothelioma. One patient underwent high ligation of the patent processus vaginalis and PLTV sheath fenestration, but one year later, he faced a recurrence. An elective second surgery was conducted via scrotal incision and Jaboulay operation was performed. The latter methodology was our treatment choice in other 7 out of 8 patients. During a 2-year postoperative follow-up, no other patient had any recurrence. We conclude that in primary hydrocele with macroscopic features indicative of tunica vaginalis inflammation, reversion of the tunica should be a part of operative strategy instead of sheath fenestration, in order to minimize the recurrence.


Assuntos
Membrana Serosa/patologia , Hidrocele Testicular/cirurgia , Adolescente , Criança , Pré-Escolar , Hemorragia/patologia , Humanos , Hiperplasia , Inflamação/patologia , Masculino , Estudos Prospectivos , Membrana Serosa/cirurgia
13.
Rev Med Brux ; 39(4): 352-358, 2018.
Artigo em Francês | MEDLINE | ID: mdl-30321000

RESUMO

High-risk oncogenic HPVs (HR-HPV) are associated in men with pre-cancerous anal dysplasia, oropharyngeal, anal and penile cancer. Anogenital warts are induced by low-risk HPVs. These manifestations are increasing among men, and especially in some high-risk groups as men who have sex with men (MSM). This review targets HPV-associated disease epidemiology as well as safety, immunogenicity, and efficacy level of HPV vaccine in men. Obstacle and cost-effectiveness analysis of HPV vaccination are discussed. Three HPV vaccines are currently available in Belgium with the 9-valent (" 9HPV " - 6/11/16/18/31/33/45/52/58) offering protection against most of HPVassociated diseases. The safe 9-valent vaccine is efficient to prevent genital warts, anal dysplasia and it decreases the recurrence of genital warts and high grade anal neoplasia in MSM with or without HIV infection. In Europe, the 9-valent vaccine could prevent in men more than 350,000 genital warts, 5,485 oropharyngeal cancers, 2,303 anal cancers et 852 grade 2/3 intraepithelial neoplasia as well as 1,113 penile cancers per year. In the Federation Wallonie-Bruxelles, the vaccine coverage reaches currently 30 % in girls and is very low in boys and men.The Superior Health Council of Belgium (CSS) recommends since 2017 the gender-neutral HPV vaccination for people up to 26 years old and to immunocompromised patients. The implementation of the CSS HPV vaccine program and its acceptability among boys and men are discussed on the basis of the most recent epidemiologic data and available costeffectiveness analysis. Ways to overcome barriers to gender-neutral HPV vaccination are suggested.


Chez l'homme, l'infection chronique par les HPV à haut risque oncogénique cause des lésions dysplasiques précancéreuses anales, des cancers oropha-ryngés, anaux et du pénis. Les HPV à bas risque oncogénique provoquent des condylomes ano-génitaux. Ces manifestations sont en augmenta-tion, notamment dans certains groupes, comme les hommes ayant des relations sexuelles avec des hommes (HSH). Cette revue de la littérature cible, l'épidémiologie des affections associées à l'HPV, la sécurité et l'efficacité des vaccins anti-HPV chez l'homme, ainsi que l'analyse des barrières à la vaccination et des études " coût-efficacité ". Des trois vaccins contre le HPV disponibles en Belgique, le Nonavalent (" 9HPV " - 6/11/16/18/31/ 33/45/52/58) offre la plus large protection. Le vaccin 9HPV est sécuritaire et prévient l'apparition de condylomes et de dysplasies anales ; il est efficace dans la prévention secondaire de condylomes et de lésions anales précancéreuses chez les HSH, qu'ils soient ou non infectés par le VIH. En Europe, chez l'homme, le 9HPV pourrait prévenir par an plus de 350.000 condylomes, 5.485 cancers oropharyngés, 2.303 cancers anaux et 852 néoplasies intra-épithéliales de grade 2/3 ainsi que 1.113 cancers du pénis. En Fédération Wallonie-Bruxelles, la couverture vaccinale est actuellement de 30 % chez les filles et anecdotique chez les garçons et les hommes. En 2017, le Conseil supérieur de la Santé (CSS) a élargi la vaccination aux deux sexes jusqu'à 26 ans et aux patients immunocompromis. L'application de ce programme de vaccination et son acceptation parmi les garçons et les hommes sont discutées sur base des données épidémiologiques récentes et des études coût-efficacité disponibles, afin d'encourager cette implémentation.


Assuntos
Infecções por Papillomavirus/prevenção & controle , Vacinas contra Papillomavirus , Adolescente , Adulto , Criança , Feminino , Humanos , Masculino , Guias de Prática Clínica como Assunto , Fatores Sexuais , Adulto Jovem
14.
J Youth Adolesc ; 46(10): 2230-2240, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28664312

RESUMO

Youth development programs represent key tools in the work of youth-serving practitioners and researchers who strive to promote character development and other attributes of youth thriving, particularly among youth who may confront structural and social challenges related to their racial, ethnic, and/or economic backgrounds. This article conducts secondary analyses of two previously reported studies of a relatively recent innovation in Boy Scouts of America (BSA) developed for youth from low-income communities, Scoutreach. Our goal is to provide descriptive and admittedly preliminary exploratory information about whether these data sets-one involving a sample of 266 youth of color from socioeconomically impoverished communities in Philadelphia (M age = 10.54 years, SD = 1.58 years) and the other involving a pilot investigation of 32 youth of color from similar socioeconomic backgrounds in Boston (M age = 9.97 years, SD = 2.46 years)-provide evidence for a link between program participation and a key indicator of positive development; that is, character development. Across the two data sets, quantitative and qualitative evidence suggested the presence of character development among Scoutreach participants. Limitations of both studies are discussed and implications for future longitudinal research are presented. We suggest that future longitudinal research should test the hypothesis that emotional engagement is key to creating the conditions wherein Scoutreach participation is linked to character development.


Assuntos
Caráter , Comportamento Infantil/psicologia , Participação da Comunidade/psicologia , Etnicidade/estatística & dados numéricos , Desenvolvimento da Personalidade , Criança , Desenvolvimento Infantil , Humanos , Masculino , Organizações sem Fins Lucrativos , Estados Unidos
15.
Folia Med Cracov ; 57(2): 53-62, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29121037

RESUMO

Transient testicular torsion (TTT) occurs when the torsion of the spermatic cord is reversed automatically within few minutes, with subsequent restoration of the blood ow to the suffering testis. e main clinical manifestation is acute scrotal pain, which resolves within a short period of time, usually few minutes. In 25% of patients su er from nausea and vomiting, besides the scrotal discomfort. Episodes of torsion can be repeated 1-30 times, leading progressively to development of ischemic trauma of the testis, while in 30-61% of all cases they constitute a precursor of testicular torsion. From January, 2016 to December, 2016, 11 patients in total were admitted to the Emergency Department due to acute scrotal pain that lasted a few minutes (1-5 minutes in most), which had already elapsed at the time of their admission, accompanied with nausea in all patients and vomiting in 5 of them. No swelling or rubor of the scrotum was revealed during physical examination, while in 9 patients it was observed that the suffering testis had transverse orientation. Ultrasonography was negative for pseudotumor or Whirlpool sign, while transverse orientation of the testis was confirmed in 9 patients. All the patients underwent surgical investigation of the suffering hemiscrotum, while Bell Clapper Deformity was found in 9 patients. Fixation of the suffering testis to the mesoscrotal diaphragm with 3 separate sutures by using non-absorbable suture followed. By the same surgical approach, the contralateral hemiscrotum was also investigated. Bilateral high adhesion of the tunica vaginalis was found in 8 out of 9 patients, in whom preventive unilateral orchidopexy was performed. All the patients are followed-up on a 6-month basis, without report of a similar, transient episode of acute scrotal pain. TTT should always be included in differential diagnosis in cases of acute scrotal pain in the past, with transverse orientation of the suffering testis. Prompt diagnosis and early treatment of the subject anatomic deformity (Bell Clapper Deformity) prevents the ischemic consequences on testicular parenchyma due to either recurrent episode of TTT or as a consequence of intravaginal testicular torsion.


Assuntos
Torção do Cordão Espermático/diagnóstico , Torção do Cordão Espermático/cirurgia , Testículo/irrigação sanguínea , Humanos , Masculino , Exame Físico , Estudos Prospectivos , Torção do Cordão Espermático/patologia
16.
Pol Merkur Lekarski ; 43(255): 120-124, 2017 Sep 29.
Artigo em Polonês | MEDLINE | ID: mdl-28987044

RESUMO

Increasing numbers of hearing pathology is auditory processing disorders. Auditory Processing Disorders (APD) are defined as difficulty in using auditory information to communicate and learn in the presence of normal peripheral hearing. It may be recognized as a problem with understanding of speech in noise and perception disorder of distorted speech. APD may accompany to articulation disorders, language problems and difficulties in reading and writing. The diagnosis of auditory processing disorders causes many difficulties primarily due to the lack of common testing procedures, precise criteria for qualification to the group of norm and pathology. The Brain-Boy Universal Professional (BUP) is one of diagnostics tools. It enables to assess the higher auditory functions. AIM: The aim of the study was preliminary assessment of hearing difficulties that may suggest the occurrence of auditory processing disorders in children. The questionnaire of hearing difficulties and BUP was used. MATERIALS AND METHODS: Study includes 20 participants 2nd grade students of elementary school. The examination of the basic central functions was carried out with BUP. The parents and teacher complete the questionnaire to evaluate the hearing problems. RESULTS: Studies carried out indicate that the 40% schoolchild have hearing difficulties. The high percentage of deficits in auditory functions was confirmed with research results of medical device and the questionnaire for teacher. CONCLUSIONS: On the basis of the studies conducted may establish that the Warnke Method can serve as preliminary assessment of hearing difficulties that may suggest the occurrence of auditory processing disorders in children.


Assuntos
Transtornos da Percepção Auditiva/diagnóstico , Transtornos da Percepção Auditiva/epidemiologia , Criança , Perda Auditiva , Humanos , Polônia/epidemiologia , Inquéritos e Questionários
17.
Am J Community Psychol ; 57(1-2): 73-86, 2016 03.
Artigo em Inglês | MEDLINE | ID: mdl-27217313

RESUMO

We examined links among three dimensions of youth involvement (intensity, duration, and engagement) in Boy Scouts of America (BSA), an international out-of-school time (OST) youth development program designed to promote moral and performance character in boys. Using data from 737 youth and their parents who participated in one of 40 BSA program sites (commonly referred to as "packs"), we first considered how individual- and pack-level measures of program involvement were differentially linked with character development. Next, we examined whether pack-level involvement characteristics moderate individual-level involvement characteristics, hypothesizing that highly involved packs would serve to further enhance the positive effects of high levels of individual involvement. Results indicated engagement was the strongest, most frequent predictor of increases in both moral and performance character. Although there were no direct effects of pack-level intensity, duration, or engagement, the effects of individual-level engagement were moderated by pack-level engagement, suggesting that the largest increases in moral and performance character occurred among highly engaged youth who were enrolled in highly engaged packs. These results highlight the need to examine multiple dimensions of OST program involvement simultaneously, and suggest that strengthening youth engagement in programming may provide a means for enhancing the positive effects of high-quality youth programming.


Assuntos
Participação da Comunidade , Motivação , Organizações sem Fins Lucrativos , Desenvolvimento da Personalidade , Criança , Estudos de Coortes , Humanos , Estudos Longitudinais , Masculino , Avaliação de Processos e Resultados em Cuidados de Saúde
18.
J Hum Evol ; 80: 74-82, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25449954

RESUMO

Because of its completeness, the juvenile Homo ergaster/erectus KNM-WT 15000 has played an important role in studies of the evolution of body form in Homo. Early attempts to estimate his adult body size used modern human growth models. However, more recent evidence, particularly from the dentition, suggests that he may have had a more chimpanzee-like growth trajectory. Here we re-estimate his adult stature and body mass using ontogenetic data derived from four African ape taxa: Pan troglodytes troglodytes, Pan troglodytes schweinfurthii, Pan paniscus, and Gorilla gorilla gorilla. The average percentage change in femoral and tibial lengths and femoral head breadth between individuals at the same stage of dental development as KNM-WT 15000 - eruption of M2s but not M3s - and adult individuals with fully fused long bone epiphyses, was determined. Results were then applied to KNM-WT 15000, and his adult size estimated from skeletal dimensions using modern human prediction formulae. Using this approach, adult stature best estimates of 176-180 cm and body mass best estimates of 80-83 kg were obtained. These estimates are close to those estimated directly from longitudinal changes in body length and body mass between 8 and 12 years of age in chimpanzees, the suggested chronological equivalent to KNM-WT 15000's remaining growth period. Thus, even using an African ape growth model, it is likely that KNM-WT 15000 would have attained close to 180 cm in stature (without a slight reduction for his lower cranial height) and 80 kg in body mass as an adult. Other evidence from the East African Early Pleistocene indicates that KNM-WT 15000 was not unusually large-bodied for his time period.


Assuntos
Tamanho Corporal , Fósseis , Hominidae/crescimento & desenvolvimento , Animais , Dentição , Gráficos de Crescimento , Masculino
19.
Cir Pediatr ; 28(2): 99-101, 2015 Apr 15.
Artigo em Espanhol | MEDLINE | ID: mdl-27775290

RESUMO

INTRODUCTION: Gastric volvulus is rare in the pediatric population. CLINICAL CASE: We report here a case of a patient of 5 years of age. COMMENTS: For its rarity, it requires a high degree of suspicion by the clinician, making it generally diagnosed very late which increases mortality.


INTRODUCCION: El vólvulo gástrico es una entidad rara en la población pediátrica. CASO CLINICO: Reportamos aquí un caso en un paciente de 5 años de edad. COMENTARIOS: Por su rareza, requiere de un alto grado de sospecha por parte del clínico, lo que hace que generalmente se diagnostique muy tardíamente, lo que incrementa la mortalidad.

20.
Pediatr Int ; 56(5): 763-7, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24628782

RESUMO

BACKGROUND: The aim of the present cross-sectional study was to investigate the relationship of physical activity level to bone mineral parameters in 11-13-year-old boys. METHODS: In total, 264 boys, divided into normal weight (n = 154) and overweight (n = 110), participated in this study. Physical activity was measured via 7 day accelerometry and bone mineral parameters using dual-energy X-ray absorptiometry. RESULTS: In overweight boys, vigorous physical activity was associated with total bone mineral density (BMD), total bone mineral content (BMC), while moderate-vigorous physical activity MVPA was associated with femoral neck BMD. In normal weight boys, however, only vigorous physical activity was associated with femoral neck BMD. When the normal weight group was divided into tertiles according to MVPA, femoral neck BMD was higher in the highest tertile compared to the lowest tertile. No other significant differences were found in bone mineral parameters according to the tertiles of MVPA. CONCLUSIONS: In overweight peripubertal boys, physical activity is more associated with bone mineral parameters compared to normal weight subjects. In addition to vigorous physical activity, moderate physical activity has a significant impact on bone mineral parameters in overweight subjects.


Assuntos
Densidade Óssea , Atividade Motora/fisiologia , Adolescente , Osso e Ossos , Criança , Estudos Transversais , Humanos , Masculino , Sobrepeso/fisiopatologia , Puberdade
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