Waardenburg syndrome: A report of three cases.
Indian J Dermatol Venereol Leprol
;
2010 Sept-Oct; 76(5): 550-552
Artículo
en Inglés
| IMSEAR
| ID: sea-140692
ABSTRACT
Waardenburg syndrome (WS) is a rare autosomally inherited and genetically heterogeneous disorder of neural crest cell development with distinct cutaneous manifestations. Based on the clinical presentations, four subtypes of the disease are recognized. A careful clinical evaluation is required to differentiate various types of WS and other associated auditory-pigmentary syndromes. We describe a case series of WS to highlight the wide spectrum of manifestations of the syndrome including a rare association.
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IMSEAR (Asia Sudoriental)
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Inglés
Revista:
Indian J Dermatol Venereol Leprol
Año:
2010
Tipo del documento:
Artículo
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