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Waardenburg syndrome

Waardenburg syndrome (WS) is a disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes.

Cerebellar dysplasia

The presence of developmental dysplasia of the cerebellum.

Total: 1

(per page)

PMID (PMCID)
19926145	MALE	Infant
	Dysplasia of the cerebellum in Waardenburg syndrome: outcomes following cochlear implantation.
	Kaufmann L, Sauter TB, Lee DJ. Int J Pediatr Otorhinolaryngol. 2010;74(1):93-6.
	This study provides the first description of isolated cerebellar dysplasia associated with Waardenburg syndrome (WS) and includes a review of cochlear implant outcomes in 42 WS patients.