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1.
Indian J Microbiol ; 62(2): 234-241, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35462705

RESUMO

Excessive use of antibiotics has led to an increase of pathogenic bacteria with multiple antibiotic resistance. Hypersaline and hyperthermal environments promote the development of several microorganisms that can potentially act as immunostimulants. Thus, the aim of this study was bioprospecting marine bacteria from these environments using mouse leukocytes as a cell model for assess immunostimulatory activity. Samples were taken from two evaporation ponds with 4 and 8% salinity (p/v) in a marine solar saltern (MSS) at Laguna Ojo de Liebre, Guerrero Negro and a shallow hydrothermal vent (SHV), Bahía Concepción under a mangrove forest both off Baja California Sur, México. From total number of isolates (N = 340), 267 were obtained from the MSS and 73 from the SHV. The 10 isolates that induced nitric oxide (NO) production in mouse splenocytes were identified using the 16S rRNA gene, of which Halomonas elongata, Halomonas sp., Pseudoalteromonas ruthenica, Bacillus subtilis and three Bacillus strains were isolated from the MSS ponds at 8% salinity and three Marinobacter lutaoensis strains from the SHV. Most of the selected bacteria were not cytotoxic for mouse splenocytes and enhanced phagocytic respiratory burst and antioxidant enzyme activities compared to the control immunostimulant (lipopolysaccharide from Escherichia coli). Selected bacteria from 8% salinity ponds in the MSS in Guerrero Negro had immunostimulant activity in vitro in mouse splenocytes. In conclusion, Bacillus subtilis SA4 220, Bacillus sp. SA4 62A, P. ruthenica SA4 40 as well as Halomonas sp. SA4 207 and Halomonas elongata SA8 44 increased several immunological parameters. Further research is needed to evaluate their potential application in preclinical models to fight against infectious diseases. Supplementary Information: The online version contains supplementary material available at 10.1007/s12088-022-01002-3.

2.
Fish Shellfish Immunol ; 84: 756-767, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-30368027

RESUMO

Gold nanoparticles (AuNP) stimulate immune responses in mammals but they have not been tested in species of relevance in aquaculture. In this study the immunostimulant and protective potential of orally administered AuNP against V. parahaemolyticus, the causative agent of Acute Hepatopancreatic Necrosis Disease, was determined in shrimp. Synthetized AuNP (18.57 ±â€¯4.37 nm) were moderately dispersed with a negative ζ potential of -10.3 ±â€¯0.208 mV (pH = 7). AuNP were administered (single dose) at 0.2, 2, and 20 µg/g feed in shrimp. Hemolymph samples were withdrawn daily for 6 days. Hemolymph or hemocytes were used to determine total hemocyte counts, immune-related enzymatic activities, and expression of immune-relevant genes. Hepatopancreas was sampled for the analysis of AuNP biodistribution and histological examination. Survival was recorded daily. No mortality or toxicity signs in hepatopancreas were found. AuNP were detected in hepatopancreas. Early (24-48 h) immunostimulation was mainly related to immune gene up-regulation. Upon a challenge with V. parahaemolyticus, survival was higher (80%) and histopathological damages were lower in shrimp treated with the 2 µg/g dose when compared to the control. Therefore orally administered AuNP are proposed as immunostimulants that protect shrimp against V. parahaemolyticus infection.


Assuntos
Adjuvantes Imunológicos/farmacologia , Ouro/farmacologia , Nanopartículas Metálicas , Penaeidae/imunologia , Substâncias Protetoras/farmacologia , Vibrio parahaemolyticus/efeitos dos fármacos , Adjuvantes Imunológicos/administração & dosagem , Animais , Ouro/administração & dosagem , Nanopartículas Metálicas/administração & dosagem , Penaeidae/efeitos dos fármacos , Substâncias Protetoras/administração & dosagem , Distribuição Tecidual , Vibrio parahaemolyticus/fisiologia
3.
Clin Otolaryngol ; 44(3): 219-226, 2019 05.
Artigo em Inglês | MEDLINE | ID: mdl-29905001

RESUMO

OBJECTIVES: To compare the outcome of the Epley maneuver (EM) in benign paroxysmal positional vertigo of the posterior canal (CSP-BPPV) depending on the definition used for recovery. DESIGN: Multicenter observational prospective study. SETTING: Otoneurology Units of 5 tertiary reference hospitals. PARTICIPANTS: All patients presenting with unilateral CSP-BPPV assisted for 1-year period. EXCLUSION CRITERIA: Spontaneous nystagmus, positive McClure-Pagnini maneuver, positive bilateral Dix-Hallpike maneuver (DHM), positive DHM for vertigo but negative for nystagmus and atypical nystagmus. MAIN OUTCOME MEASURES: Response to EM was measured after 7 days in 3 different outcomes: disappearance of nystagmus during the DHM in the follow-up visit, disappearance of vertigo during the DHM and general status (GS) during daily life activities. RESULTS: 264 patients were recruited (68 male/166 female, mean age 62 years). After the EM, nystagmus disappeared in 67% of them, vertigo in 54% and 36% were asymptomatic in their daily life. These outcomes were strongly correlated, but they were not concordant in a clinically significant group of cases; only the 26% of patients met all of them. The healing process follows the next sequence: negativization of positional nystagmus, then disappearance of positional vertigo and, finally, the improvement of GS during daily life activities. CONCLUSION: Nowadays, healing criteria for the resolution of an PSC-BPPV episode have not been specifically defined yet. Provided that other otoneurological disorders have been ruled out, the next resolution criterion is proposed: absence of nystagmus and specifically during control DHM and disappearance of symptoms during daily life activities.


Assuntos
Atividades Cotidianas , Vertigem Posicional Paroxística Benigna/diagnóstico , Postura/fisiologia , Recuperação de Função Fisiológica , Canais Semicirculares/fisiopatologia , Vertigem Posicional Paroxística Benigna/fisiopatologia , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Prognóstico , Estudos Prospectivos , Testes de Função Vestibular
4.
J Helminthol ; 93(1): 57-65, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29248015

RESUMO

The toxicity of water-ethanol extracts of garlic (Allium sativum), ginger (Zingiber officinale), basil (Ocimum basilicum), bitter chaparro (Castela tortuousa), onion (Allium cepa) and papaya (Carica papaya) against adults, eggs and oncomiracidia of Neobenedenia spp. parasites was examined. Parasites were exposed to continuous immersion and treated as follows: extracts were tested at three dilutions: 1:10, 1:50 and 1:100 made with filtered seawater (35 g l-1); ethanol (70%) was evaluated at the same dilutions of 1:10 (7% ethanol), 1:50 (1.4% ethanol) and 1:100 (0.07% ethanol) and a seawater (35 g l-1) control. The antiparasitic effect was measured on: (1) adult survival, egg production and time to detachment from the culture vessel; (2) egg development and cumulative egg hatching; and (3) oncomiracidia survival. All three dilutions of ginger and dilutions 1:100 and 1:50 of basil extract reduced adult survival in vitro, time to detachment from the surface of the culture vessel, egg production and oncomiracidia survival. Bitter chaparro extract reduced adult egg production and oncomiracidia survival. Hatching success was significantly reduced (P < 0.05) in basil extract (1:100) to 86.6% compared to the seawater control (100%). Dilutions 1:10 of ginger and basil exhibited the highest impact on the biological parameters of Neobenedenia sp. Our study demonstrates that water-ethanol extracts of ginger, basil and bitter chaparro are toxic against Neobenedenia sp. life stages.


Assuntos
Ectoparasitoses/veterinária , Doenças dos Peixes/tratamento farmacológico , Helmintíase Animal/tratamento farmacológico , Extratos Vegetais/farmacologia , Extratos Vegetais/uso terapêutico , Trematódeos/efeitos dos fármacos , Animais , Antiplatelmínticos/farmacologia , Antiplatelmínticos/uso terapêutico , Ectoparasitoses/tratamento farmacológico , Ectoparasitoses/parasitologia , Doenças dos Peixes/parasitologia , Helmintíase Animal/parasitologia , Magnoliopsida/química , Óvulo/efeitos dos fármacos , Óvulo/fisiologia , Trematódeos/fisiologia
5.
J Fish Dis ; 40(11): 1497-1509, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-28422295

RESUMO

Neobenedenia melleni is a monogenean parasite that causes significant mortality and economic losses in fish aquaculture. Changes in the antigenic composition of this parasite occur during its developmental stages. In this study, we evaluated humoral parameters in serum and transcriptional immune responses of yellowtail naturally infected with N. melleni. In addition, in vitro assays were performed to study the stimulatory effects of antigens from larvae and adults on spleen leucocytes from non-infected fish at 6 and 24 h post-stimulation. The results showed enhanced total protein, myeloperoxidase and antiprotease activities in N. melleni-infected fish compared with non-infected ones. The induction of Toll-like receptors (TLRs) and pro-inflammatory cytokines in spleen leucocytes during natural infection with N. melleni suggests that these immune-related genes play an important role in the initiation of the immune defence mechanism for controlling parasite infection. Interestingly, the magnitude of in vitro responses of spleen leucocytes was dependent on the parasitic stage. An important stimulation of gene expression by adult antigens on spleen leucocytes was observed. Differential expression patterns of TLRs and target cytokines in yellowtail leucocytes in both in vivo and in vitro studies suggest that the quality of yellowtail immune response is conditioned by N. melleni development.


Assuntos
Antígenos de Helmintos/imunologia , Doenças dos Peixes/imunologia , Imunidade Humoral , Imunidade Inata , Perciformes , Trematódeos/imunologia , Infecções por Trematódeos/veterinária , Animais , Citocinas/genética , Citocinas/metabolismo , Doenças dos Peixes/parasitologia , Proteínas de Peixes/genética , Proteínas de Peixes/metabolismo , Larva/genética , Larva/imunologia , Leucócitos/metabolismo , Baço/metabolismo , Receptores Toll-Like/genética , Receptores Toll-Like/metabolismo , Trematódeos/crescimento & desenvolvimento , Infecções por Trematódeos/imunologia , Infecções por Trematódeos/parasitologia
6.
Eur Arch Otorhinolaryngol ; 274(10): 3567-3576, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28725982

RESUMO

Benign paroxysmal positional vertigo (BPPV) is the most frequent type of vertigo. The treatment of canalithiasis of the posterior semicircular canal consists in performing a particle-repositioning maneuver, such as the Epley maneuver (EM). However, the EM is not effective in all cases. The objective of this study is to identify risk factors, which predict the EM failure, among the clinical variables recorded in anamnesis and patient examination. This is an observational prospective multicentric study. All patients presenting with BPPV were recruited and applied the EM and appointed for a follow-up visit 7 days later. The following variables were recorded: sex, age, arterial hypertension, diabetes, hyperlipidemia, smoking habit, alcohol consumption, migraine, osteoporosis, diseases of the inner ear, previous ipsilateral BPPV, previous traumatic brain injury, previous sudden head deceleration, time of evolution, sulpiride or betahistine treatment, experienced symptoms, outcome of the Halmagyi maneuver, laterality, cephalic hyperextension of the neck, intensity of nystagmus, intensity of vertigo, duration of nystagmus, occurrence of orthotropic nystagmus, symptoms immediately after the EM, postural restrictions, and symptoms 7 days after the EM. Significant differences in the rate of loss of nystagmus were found for six variables: hyperlipidemia, previous ipsilateral BPPV, intensity of nystagmus, duration of nystagmus, post-maneuver sweating, and subjective status. The most useful significant variables in the clinical practice to predict the success of the EM are previous BPPV and intensity of nystagmus. In the other significant variables, no physiopathological hypothesis can be formulated or differences between groups are too small.


Assuntos
Vertigem Posicional Paroxística Benigna , Nistagmo Patológico , Posicionamento do Paciente/métodos , Canais Semicirculares , Adulto , Vertigem Posicional Paroxística Benigna/fisiopatologia , Vertigem Posicional Paroxística Benigna/terapia , Feminino , Lateralidade Funcional , Humanos , Masculino , Pessoa de Meia-Idade , Nistagmo Patológico/diagnóstico , Nistagmo Patológico/fisiopatologia , Prognóstico , Estudos Prospectivos , Fatores de Risco , Canais Semicirculares/patologia , Canais Semicirculares/fisiopatologia , Resultado do Tratamento
7.
Radiologia ; 58(1): 26-37, 2016.
Artigo em Espanhol | MEDLINE | ID: mdl-26433623

RESUMO

Malignant heart tumors are less common than benign ones. They can be primary or secondary. Secondary or metastatic heart tumors are 20 to 40 times more common than primary malignant heart tumors, which have an estimated incidence of 0.05%. Non-neoplastic pseudotumors can present as cardiac masses, with imaging characteristics than can suggest the diagnosis of a tumor. The aim of this article is to describe and illustrate malignant heart tumors and pseudotumors, stressing the CT and MRI findings that make it possible to differentiate them from benign cardiac tumors.


Assuntos
Neoplasias Cardíacas/diagnóstico por imagem , Imageamento por Ressonância Magnética , Tomografia Computadorizada por Raios X , Diagnóstico Diferencial , Humanos
8.
Genet Mol Res ; 14(4): 11848-59, 2015 Oct 02.
Artigo em Inglês | MEDLINE | ID: mdl-26436509

RESUMO

Copy number variations (CNVs) are an important source of genomic structural variation, and can be used as markers to investigate phenotypic and economic traits. CNVs also have functional effects on gene expression and can contribute to disease susceptibility in mammals. Currently, single nucleotide polymorphism genotyping arrays (SNP chips) are the technology of choice for identifying CNV variations. Microarray technologies have recently been used to study the bovine genome. The objective of the present study was to develop CNVs in Holstein cows from the Northwest of Mexico using the Affymetrix Axiom Genome-Wide BOS 1 Array, which assays 648,315 SNPs and provides a wide coverage for genome-wide studies. We applied the two most widely used algorithms for the discovery of CNVs (PennCNV and QuantiSNP) and found 56 CNV regions (CNVRs) representing 0.33% of the bovine genome (8.46 Mb). These CNVRs ranged from 1.5 to 970.8 kb with an average length of 151 kb. They involved 103 genes and showed a 28% overlap with CNVRs already reported. Of the 56 CNVRs found, 20 were novel. In this study we present the first genomic analysis of CNVs in Mexican cattle using high-density SNP data. Our results provide a new reference basis for future genomic variation and association studies between CNVs and phenotypes, especially in Mexican cattle.


Assuntos
Algoritmos , Variações do Número de Cópias de DNA , Genoma , Polimorfismo de Nucleotídeo Único , Característica Quantitativa Herdável , Animais , Bovinos , Indústria de Laticínios , Feminino , Genótipo , Técnicas de Genotipagem , Humanos , México , Análise de Sequência com Séries de Oligonucleotídeos , Fenótipo
9.
Ginecol Obstet Mex ; 83(7): 422-8, 2015 Jul.
Artigo em Espanhol | MEDLINE | ID: mdl-26422913

RESUMO

OBJECTIVES: To evaluate the effectiveness of the hysteroscopic polypectomy in terms of the decrease of the abnormal uterine bleeding. METHODS: A cross-sectional and analytical study was done with patients to whom a hysteroscopic polypectomy was done for treating the abnormal uterine bleeding, between January 2009 and December 2013. The response to the treatment was evaluated via a survey given to the patients about the behavior of the abnormal uterine bleeding after the procedure and about overall satisfaction. RESULTS: The results were obtained after a hysteroscopic polypectomy done to 128 patients and were as follows. The average time from the polypectomy applied until the survey was 30.5 months, with a standard deviation of 18 months. 67.2% of the patients reported decreased abnormal uterine bleeding and the 32.8% reported a persistence of symptoms. On average 82.8% of the. patients were satisfied with the treatment. Bivariate and multivariate analysis showed no association between the variables studied and no improvement of abnormal uterine bleeding after surgery (polypectomy). There were no complications. CONCLUSION: Hysteroscopic polypectomy is a safe surgical treatment, which decreases on two of three patients the abnormal uterine bleeding in the presence of endometrial polyps, with an acceptable level of satisfaction.


Assuntos
Histeroscopia/métodos , Pólipos/cirurgia , Doenças Uterinas/cirurgia , Hemorragia Uterina/cirurgia , Adulto , Estudos Transversais , Coleta de Dados , Feminino , Humanos , Pessoa de Meia-Idade , Análise Multivariada , Satisfação do Paciente , Pólipos/complicações , Fatores de Tempo , Resultado do Tratamento , Doenças Uterinas/patologia , Hemorragia Uterina/patologia
10.
Radiologia ; 57(6): 480-8, 2015.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-26307666

RESUMO

Cardiac masses represent a diagnostic challenge because decisions about treatment are based on imaging techniques. Echocardiography, magnetic resonance (MR) and computed tomography (CT) are fundamental for the detection, characterization, and staging of cardiac masses as well as for planning their treatment. Most primary cardiac tumors are benign; myxomas, papillary fibroelastomas, and lipomas are the most common. The location of the tumors and its characteristics on CT and MR orient the etiologic diagnosis in most cases. This article describes the protocols for CT and MR studies of cardiac masses as well as the morphologic findings, predominant locations, and most useful characteristics for characterizing benign cardiac masses and establishing the differential diagnosis with malignant cardiac tumors and non-neoplastic pseudotumors.


Assuntos
Neoplasias Cardíacas/diagnóstico por imagem , Lipoma/diagnóstico por imagem , Mixoma/diagnóstico por imagem , Ecocardiografia , Humanos , Imageamento por Ressonância Magnética , Tomografia Computadorizada por Raios X
12.
Nature ; 431(7010): 823-6, 2004 Oct 14.
Artigo em Inglês | MEDLINE | ID: mdl-15483606

RESUMO

Quantum tunnelling through a potential barrier (such as occurs in nuclear fusion) is very sensitive to the detailed structure of the system and its intrinsic degrees of freedom. A strong increase of the fusion probability has been observed for heavy deformed nuclei. In light exotic nuclei such as 6He, 11Li and 11Be (termed 'halo' nuclei), the neutron matter extends much further than the usual nuclear interaction scale. However, understanding the effect of the neutron halo on fusion has been controversial--it could induce a large enhancement of fusion, but alternatively the weak binding energy of the nuclei could inhibit the process. Other reaction channels known as direct processes (usually negligible for ordinary nuclei) are also important: for example, a fragment of the halo nucleus could transfer to the target nucleus through a diminished potential barrier. Here we study the reactions of the halo nucleus 6He with a 238U target, at energies near the fusion barrier. Most of these reactions lead to fission of the system, which we use as an experimental signature to identify the contribution of the fusion and transfer channels to the total cross-section. At energies below the fusion barrier, we find no evidence for a substantial enhancement of fusion. Rather, the (large) fission yield is due to a two-neutron transfer reaction, with other direct processes possibly also involved.

13.
J Otol ; 14(3): 111-116, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31467509

RESUMO

BACKGROUND: Probable benign paroxysmal positional vertigo, spontaneously resolved (pBPPVsr), is a variant of benign paroxysmal positional vertigo (BPPV) in which there is no observable nystagmus and no vertigo with any positional maneuver. OBJECTIVES: To calculate the incidence pBPPVsr, compare the characteristics of the patients with pBPPVsr and BPPV not spontaneously resolved and describe the spontaneous resolution in the natural course of BPPV. METHODS: Multicenter prospective descriptive study. During a one-year period, all patients with suspected BPPV that presented to the Neurotology Units of five participating centers were recruited. The incidence of pBPPVsr was calculated as a percentage of the total number of patients with BPPV. The prevalence of several variables was compared between pBPPVsr and BPPV not spontaneously resolved. The timing of spontaneous resolution was estimated using Kaplan-Meier curves. RESULTS: 457 patients met the inclusion criteria. The incidence of pBPPVsr was 33.5%. It was significantly higher in males, in patients with normal bone mass and in patients who were not taking sulpiride. A rate of 18% of spontaneous resolution after the first month and 51% after the first year was found. This percentage did not change in a significant way after this moment. The curves for males, patients under 50 and patients with normal blood pressure decreased significantly faster. CONCLUSIONS: In our serie, BPPV spontaneously resolved in half of the patients with BPPV during the first year. This seemed to occur more commonly in males and could have been hindered by sulpiride intake, osteoporosis, advanced age and high blood pressure.

14.
Clin Genet ; 73(3): 262-7, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18177466

RESUMO

Branchio-oto-renal (BOR) and Stickler (STL) syndromes are disorders that include hearing loss among their clinical features. STL syndrome type I (STL1) is a combination of ophthalmic, orofacial, articular, and auditory manifestations, caused by mutations in the COL2A1. BOR syndrome is an autosomal dominant trait encompassing branchial, otic and renal anomalies because of mutations in EYA1, SIX1 and SIX5. In this study, we have clinically and genetically diagnosed a proband that displayed STL1 and BOR syndromes. This patient and his younger brother exhibited hearing loss and cleft palate. Both siblings and their mother also showed myopia, congenital non-progressive vitreous anomaly and a flat face. Taken together, these clinical features are consistent with the diagnosis of a familial case of STL. Sequence analysis revealed in the three patients a novel COL2A1 mutation (c.1468_1475delinsT) that accounted for a STL1 phenotype. The proband also displayed pre-auricular pits, branchial fistulae and renal agenesis that define BOR syndrome. Interestingly, this patient carries an EYA1 mutation, p.R328X, which was not present in the two other patients or in his healthy father, supporting that the mutation arose de novo. In conclusion, this report highlights the importance of molecular testing and detailed clinical evaluation for the diagnosis of syndromes with overlapping phenotypic features.


Assuntos
Anormalidades Múltiplas/genética , Síndrome Brânquio-Otorrenal/genética , Colágeno Tipo II/genética , Peptídeos e Proteínas de Sinalização Intracelular/genética , Mutação/genética , Proteínas Nucleares/genética , Proteínas Tirosina Fosfatases/genética , Adulto , Sequência de Bases , Análise Mutacional de DNA , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Linhagem , Fenótipo , Síndrome , Tomografia Computadorizada por Raios X
15.
IEEE Trans Neural Netw ; 19(4): 723-5, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18390315

RESUMO

During the usual SVM biclassification learning process, the bias is chosen a posteriori as the value halfway between separating hyperplanes. A note on different approaches on the calculation of the bias when SVM is used for multiclassification is provided and empirical experimentation is carried out which shows that the accuracy rate can be improved by using bias formulations, although no single formulation stands out as providing better performance.


Assuntos
Viés , Redes Neurais de Computação , Análise Numérica Assistida por Computador , Simulação por Computador , Humanos
16.
Acta Otorrinolaringol Esp ; 57(9): 425-8, 2006 Nov.
Artigo em Espanhol | MEDLINE | ID: mdl-17184012

RESUMO

The Velocardiofacial (VCF) syndrome is a relatively frequent cromosomopathy that usually associates various otorhinolaryngological features, as hipenasal speech, typical facies and auricular anomalies. We report a patient with VCF syndrome that before being diagnosed had undergone adenoidectomy with a postoperative worsening in speech. Otorhinolaryngological clinical features of the VCF syndrome are discussed and a diagnostic protocol is proposed to achieve an early diagnosis and to prevent iatrogenic interventions in these patients.


Assuntos
Síndrome de DiGeorge/complicações , Síndrome de DiGeorge/diagnóstico , Distúrbios da Fala/diagnóstico , Distúrbios da Fala/etiologia , Criança , Cromossomos Humanos Par 22/genética , Síndrome de DiGeorge/genética , Diagnóstico Diferencial , Feminino , Humanos , Índice de Gravidade de Doença
17.
Acta Otorrinolaringol Esp ; 57(7): 300-2, 2006.
Artigo em Espanhol | MEDLINE | ID: mdl-17036990

RESUMO

INTRODUCTION: Cerebral palsy (CP) is the most common chronic motor disorder in children and frequently associates sensorial pathology. The objective of our study was to establish the prevalence and characteristics of sensorineural hearing loss in children with CP. METHODS: We performed a retrospective study of patients born between the years 1975 and 2004, diagnosed of CP in the "Marqués de Valdecilla" University Hospital. Clinical data were collected including the presence of sensorineural hearing loss, age at diagnosis, treatment and associated pathology. RESULTS: Sixty four patients had confirmed CP. Audiological testing had been performed in thirty patients (47%) of them 18 (60%) had sensorineural hearing loss (12 bilateral and 6 unilateral). In thirteen cases hearing loss was associated with mental retardation. The age at diagnosis ranged from 3 months to 7 years (mean 23.2 months). Eight patients were treated with hearing aids and one with a cochlear implant. CONCLUSIONS: Sensorineural hearing loss is frequent in CP patients. Management of this problem is difficult in this setting because of the motor disorder and the associated pathology. Early audiological assessment is very important to improve the language outcome in these children.


Assuntos
Paralisia Cerebral/complicações , Perda Auditiva Neurossensorial/etiologia , Feminino , Perda Auditiva Neurossensorial/epidemiologia , Humanos , Masculino , Estudos Retrospectivos
18.
Acta Otorrinolaringol Esp ; 57(6): 262-5, 2006.
Artigo em Espanhol | MEDLINE | ID: mdl-16872101

RESUMO

OBJECTIVE: The objective [corrected] of our study was to assess the most frequent otorhinolaryngological manifestations in patients with Down syndrome, and to propose diagnostic and management guidelines to improve their quality of life. METHODS: Patients with Down's syndrome referred to the ENT Department of two Spanish Hospitals during a 4-year period were retrospectively reviewed. Data of the following variables were collected: main symptoms, diagnosis, comorbidities, surgical procedures, and complications. RESULTS: Thirty patients with Down's syndrome were included in our study. The most frequent reasons for referral were hearing loss and newborns from the Hearing Impairment Screening Program. Otitis media with effusion, adenoid hypertrophy and obstructive sleep apnea were the most common diagnosis. Five patients underwent head and neck surgical procedures without complications. CONCLUSIONS: Hearing loss secondary to chronic otitis media with effusion and upper airway obstruction are frequent pathologies in patients with Down syndrome.


Assuntos
Síndrome de Down/epidemiologia , Perda Auditiva/epidemiologia , Apneia Obstrutiva do Sono/epidemiologia , Adolescente , Adulto , Criança , Pré-Escolar , Feminino , Guias como Assunto , Perda Auditiva/diagnóstico , Humanos , Lactente , Recém-Nascido , Masculino , Pessoa de Meia-Idade , Prevalência , Qualidade de Vida , Estudos Retrospectivos , Índice de Gravidade de Doença , Apneia Obstrutiva do Sono/diagnóstico
19.
Acta Otorrinolaringol Esp ; 57(7): 333-5, 2006.
Artigo em Espanhol | MEDLINE | ID: mdl-17036997

RESUMO

We report an infant with auditory neuropathy secondary to the Q829X mutation in the gene encoding otoferlin (OTOF). Included in a universal newborn hearing screening program, the subject passed the otoacoustic emission (OAEs) test. Given that the infant had a familial history of deafness auditory brainstem response (ABR) testing was performed, revealing a profound hearing impairment. The genetic study confirmed that the subject was homozygous for the Q829X mutation in OTOF. The patient underwent a cochlear implant, obtaining satisfactory results. The moderately high prevalence of this mutation in the Spanish population could produce a significant false negative rate in newborn hearing screening programs using OAEs.


Assuntos
Nervo Coclear , Perda Auditiva/genética , Proteínas de Membrana/genética , Mutação , Doenças do Nervo Vestibulococlear/genética , Humanos , Lactente , Masculino
20.
Anim Reprod Sci ; 170: 157-69, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27236376

RESUMO

The granulocyte-macrophage colony stimulating factor (GM-CSF) is a multifunctional cytokine implicated in proliferation, differentiation, and activation of several cell types including those involved in hematopoiesis and reproduction. In the present study, the expression of the α- and ß-subunit genes of GM-CSF receptor during follicular development in cattle was assessed. The spatial association of α- and ß-subunits of GM-CSF with follicle stimulating hormone receptor (FSHR) and 3ß-hydroxysteroid dehydrogenase (3ß-HSD), and the temporal associations with gene expression of hexose transporters (GLUTs) in granulosa cells of cattle were also evaluated. The effect of GM-CSF on the functionality of hexose transporters was also determined in an in vitro primary culture of granulosa cells. The spatial association of subunits of the GM-CSF receptor with 3ß-HSD and FSHR suggests a potential steroidogenic regulation of GM-CSF in granulosa cells. Immunodetection of GLUTs and uptake kinetic assays confirmed expression and functionality of these genes for hexose transporters in granulosa cells of cattle. Treatment of granulosa cells with GM-CSF, FSH or insulin- like growth factor-I (IGF-I) alone increased 2-deoxyglucose (DOG) or 3-0-methylglucose (OMG) uptake; however, when cells were treated with various combination of these factors there were no additive effect. Unexpectedly, the combination of GM-CSF and FSH decreased DOG uptake compared to FSH treatment alone. Thus, the expression pattern of GM-CSF receptor subunit genes during follicle development in cattle and promotion of DOG and OMG uptake in granulosa cells indicate a role for GM-CSF, FSH and/or IGF-I alone in regulating granulosa cell metabolic activity, specifically by promoting glucose uptake.


Assuntos
Bovinos/fisiologia , Glucose/metabolismo , Células da Granulosa/efeitos dos fármacos , Folículo Ovariano/metabolismo , Receptores de Fator Estimulador das Colônias de Granulócitos e Macrófagos/fisiologia , 3-Hidroxiesteroide Desidrogenases/genética , 3-Hidroxiesteroide Desidrogenases/metabolismo , 3-O-Metilglucose/metabolismo , Animais , Desoxiglucose/metabolismo , Feminino , Hormônio Foliculoestimulante/metabolismo , Regulação da Expressão Gênica/fisiologia , Fator Estimulador de Colônias de Granulócitos e Macrófagos/metabolismo , Fator de Crescimento Insulin-Like I/metabolismo , Proteínas de Transporte de Monossacarídeos/genética , Proteínas de Transporte de Monossacarídeos/metabolismo , Subunidades Proteicas , Traçadores Radioativos , Receptores do FSH/genética , Receptores do FSH/metabolismo , Fatores de Tempo
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