Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Añadir filtros








Tipo de estudio
Intervalo de año
1.
Iranian Journal of Pediatrics. 2011; 21 (1): 121-125
en Inglés | IMEMR | ID: emr-109569

RESUMEN

Several clinical entities combine ectodermal dysplasia [ED] and cleft lip and/or palate [CL/P]. These disorders have been recognized with a narrow phenotypic spectrum and very similar clinical features. We report a case with a clinical diagnosis of Hay Wells syndrome [ankyloblepharon, ED and CL/P], who is a descendent of a mother with Bowen Armstrong syndrome [ED, CL/P, mental retardation]. Due to the clinical similarities, we suggest that Hay Wells syndrome and Bowen Armstrong syndrome may be the same clinical entity with variable manifestations. This case highlights the difficulties in trying to classify the ED syndromes on clinical features


Asunto(s)
Humanos , Masculino , Labio Leporino , Fisura del Paladar , Anomalías del Ojo , Párpados/anomalías , Discapacidad Intelectual
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA