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Curr Eye Res ; 40(9): 884-90, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25310457

RESUMO

PURPOSE: X-linked hypohidrotic ectodermal dysplasia (XLHED) is the most common form of ectodermal dysplasia. Clinical characteristics include meibomian gland disorder and the resulting hyperevaporative dry eye. In this study, we evaluated meibography and ocular infrared thermography as novel methods to diagnose XLHED. METHODS: Eight infants, 12 boys and 14 male adults with XLHED and 12 healthy control subjects were subjected to a panel of tests including the ocular surface disease index (OSDI), meibography and infrared thermography, non-invasive measurement of tear film break-up time (NIBUT) and osmolarity, Schirmer's test, lissamine green staining and fluorescein staining. Sensitivity and specificity were determined for single tests and selected test combinations. RESULTS: Meibography had 100% sensitivity and specificity for identifying XLHED. Infrared thermography, a completely non-invasive procedure, revealed a typical pattern for male subjects with XLHED. It was, however, less sensitive (86% for adults and 67% for children) than meibography or a combination of established routine tests. In adults, OSDI and NIBUT were the best single routine tests (sensitivity of 86% and 71%, respectively), whereas increased tear osmolarity appeared as a rather unspecific ophthalmic symptom. In children, NIBUT was the most convincing routine test (sensitivity of 91%). CONCLUSIONS: Meibography is the most reliable ophthalmic examination to establish a clinical diagnosis in individuals with suspected hypohidrotic ectodermal dysplasia, even before genetic test results are available. Tear film tests and ocular surface staining are less sensitive in children, but very helpful for estimating the severity of ocular surface disease in individuals with known XLHED.


Assuntos
Temperatura Corporal/fisiologia , Displasia Ectodérmica Anidrótica Tipo 1/diagnóstico , Glândulas Tarsais/metabolismo , Lágrimas/química , Termografia/métodos , Adolescente , Adulto , Criança , Pré-Escolar , Displasia Ectodérmica Anidrótica Tipo 1/genética , Displasia Ectodérmica Anidrótica Tipo 1/metabolismo , Humanos , Lactente , Recém-Nascido , Raios Infravermelhos , Masculino , Glândulas Tarsais/patologia , Glândulas Tarsais/fisiopatologia , Pessoa de Meia-Idade , Concentração Osmolar , Reprodutibilidade dos Testes , Adulto Jovem
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