Waardenburg syndrome in childhood deafness in Cameroon

BACKGROUND: Waardenburg syndrome (WS) is a rare hereditary disorder essentially characterised by deafness and pigment disorders of the eyes, hair and skin. METHODS: Between October 2010 and December 2011, we identified six patients with WS during an aetiological survey of 582 deaf participants recru...

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Veröffentlicht in:	SAJCH : the South African journal of child health 2014-02, Vol.8 (1), p.3-05
Hauptverfasser:	Noubiap, Jean-Jacques N, Djomou, Francois, Njock, Richard, Toure, Geneviève Bengono, Wonkam, Ambroise
Format:	Artikel
Sprache:	eng
Schlagworte:	Health Care Sciences & Services
Online-Zugang:	Volltext
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