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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.

Hypothalamic hamartoma

The presence of a hamartoma of the hypothalamus.

Total: 1

(per page)

PMID (PMCID)
9890185	MALE
	Cranial MR imaging findings in Waardenburg syndrome: anophthalmia, and hypothalamic hamartoma.
	Sener RN. Comput Med Imaging Graph. 1998;22(5):409-11.
	Cranial MR imaging examination findings of a three and half year old boy with Waardenburg syndrome are described which consisted of bilateral congenital anophthalmia (secondary type), and a hypothalamic hamartoma.