Waardenburg syndrome: A report of three cases.
Indian J Dermatol Venereol Leprol
;
2010 Sept-Oct; 76(5): 550-552
Article
in English
| 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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
Indian J Dermatol Venereol Leprol
Year:
2010
Type:
Article
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