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1.
Am J Med Genet A ; 173(2): 309-314, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-27774762

RESUMEN

Oculoauriculovertebral spectrum (OAVS), also known as Goldenhar syndrome, is considered a condition associated to failing of embryogenesis involving the first and second branchial arches, leading to structural abnormalities arising from it. The aim of this study is to verify the hearing features presented by patients with OAVS and provide additional information that may contribute to improvement of speech therapy. The sample consisted of 10 individuals diagnosed with OAVS and cared for by the Clinical Genetics Service. All patients underwent objective assessment of auditory function through tonal and vocal audiometry. This evaluation was completed using TOAE and BERA. The patient's age ranged from 1 year and 9 months to 27 years and 4 months. At physical examination it was found that 10 had microtia, 7 preauricular tags, 6 low-set ears, 6 ear canal atresia, and 2 preauricular pits. Among the patients, five presented with abnormal hearing. Three patients had conductive hearing loss ranging from mild to moderate, and two patients had sensorineural hearing loss from mild to profound. Three patients had hearing loss in both ears. Speech-language disorders are common in children with OAVS. Thus, the referral to the audiologist and speech pathologist is indicated as soon as possible. Early recognition and detailed understanding of aspects related to the etiology, clinical features, and outcome of patients with OAVS are essential for their proper management. © 2016 Wiley Periodicals, Inc.


Asunto(s)
Síndrome de Goldenhar/diagnóstico , Fenotipo , Adolescente , Adulto , Niño , Preescolar , Femenino , Síndrome de Goldenhar/genética , Pérdida Auditiva/diagnóstico , Pérdida Auditiva/genética , Pruebas Auditivas , Humanos , Lactante , Masculino , Examen Físico , Estudios Prospectivos , Adulto Joven
2.
Environ Monit Assess ; 186(4): 2195-204, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24292950

RESUMEN

The search for reliable biomarkers of human exposure to benzene and its derivatives is still subject of research. Many of the proposed biomarkers have limitations ranging from the low sensitivity to the wide variability of results. Thus, the aim of our study was to assess the frequencies of chromosomal abnormalities (CA) and sister chromatid exchanges (SCE) in workers of gas stations, with (cases, n = 19) and without (local controls, n = 6) risk of exposure to benzene and its derivatives, comparing them with the results from the general population (external controls, n = 38). The blood dosages of benzene, toluene, and xylenes were measured in all participants. Blood solvent levels were compared with the findings obtained in cytogenetic evaluation and a research protocol which included data of the workplace, lifestyle, and health of the individuals. We did not detect the presence of benzene and its derivatives and did not find chromosomal damage that may be associated with the gas station activity in cases. Moreover, although we found an association of increased SCE and the working time in the local controls, the values found for SCE are within normal limits. Thus, our evaluation of SCE and CA reflected the levels of benzene and its derivatives observed in the blood. We believe, therefore, that SCE and CA may actually constitute possible tests for the evaluation of these exposures. However, we believe that further studies, including individuals at risk, are important to confirm this assertion.


Asunto(s)
Contaminantes Ocupacionales del Aire/toxicidad , Benceno/toxicidad , Exposición Profesional/análisis , Adulto , Contaminantes Ocupacionales del Aire/análisis , Contaminantes Ocupacionales del Aire/metabolismo , Benceno/análisis , Benceno/metabolismo , Biomarcadores/metabolismo , Aberraciones Cromosómicas/inducido químicamente , Femenino , Gasolina/toxicidad , Humanos , Masculino , Exposición Profesional/estadística & datos numéricos , Intercambio de Cromátides Hermanas/fisiología , Adulto Joven
3.
Braz J Otorhinolaryngol ; 77(4): 455-460, 2011.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-21860971

RESUMEN

UNLABELLED: Oculo-auriculo-vertebral spectrum (OAVS) is a rare condition characterized by the involvement of the first branchial arches. PURPOSE: To investigate the ear abnormalities of a sample of patients with OAVS. MATERIALS AND METHODS: The sample consisted of 12 patients with OAVS seen at the Clinical Genetics Unit, UFCSPA/CHSCPA. The study included only patients who underwent mastoid computed tomography and with normal karyotype. We performed a review of its clinical features, giving emphasis to the ear findings. RESULTS: Nine patients were male, the ages ranged from 1 day to 17 years. Ear abnormalities were observed in all patients and involved the external (n = 12), middle (n = 10) and inner ear (n = 3). Microtia was the most frequent finding (n = 12). The most common abnormalities of the middle ear were: opacification (n = 2), displacement (n = 2) and malformation of the ossicular chain. Agenesis of the internal auditory canal (n = 2) was the most frequent alteration of the inner ear. CONCLUSIONS: Ear abnormalities are variable in patients with OAVS and often there is no correlation between findings in the external, middle and inner ear. The evaluation of these structures is important in the management of individuals with OAVS.


Asunto(s)
Pabellón Auricular/anomalías , Oído Interno/anomalías , Oído Medio/anomalías , Síndrome de Goldenhar/complicaciones , Adolescente , Niño , Preescolar , Femenino , Humanos , Lactante , Masculino , Índice de Severidad de la Enfermedad , Tomografía Computarizada por Rayos X
4.
Pediatr Int ; 53(4): 551-7, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21342361

RESUMEN

BACKGROUND: Congenital heart disease (CHD) is a serious threat to public health. Despite this, its etiology is poorly understood and few cardiac teratogens have been defined. The aim of the present study was to identify gestational and family risk factors for CHD in a sample of patients from a pediatric hospital in southern Brazil. METHODS: A prospective and consecutive sample from subjects with or without CHD, hospitalized at a pediatric intensive care unit, was enrolled. All patients with CHD underwent a GTG-banding karyotype. Chromosomal abnormalities were observed in 47 subjects (15.8%), and these were excluded from the study. The final sample consisted of 250 CHD subjects and 303 controls. RESULTS: After statistical analysis, using logistic regression, the variables age, rural location, gestational loss, use of anti-hypertensive medication, antibiotics and alcohol in the first trimester of pregnancy were all independently associated with CHD. These results were similar to those of some studies and different from others. It should be noted, however, that, for several variables, the data in the literature as well as the present study were insufficient to determine risk. CONCLUSIONS: Some differences found may be explained by genetic factors and sociocultural diversity. In contrast, because CHD consists of a heterogeneous group of lesions, the etiology may vary. The standardization of research data and classification of methods for future studies are essential.


Asunto(s)
Cardiopatías Congénitas/etiología , Anomalías Inducidas por Medicamentos/epidemiología , Anomalías Inducidas por Medicamentos/genética , Adolescente , Brasil , Niño , Preescolar , Salud de la Familia , Femenino , Cardiopatías Congénitas/inducido químicamente , Cardiopatías Congénitas/epidemiología , Cardiopatías Congénitas/genética , Humanos , Lactante , Cariotipificación , Modelos Logísticos , Masculino , Embarazo , Estudios Prospectivos , Factores de Riesgo
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