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.

Intestinal obstruction

Blockage or impairment of the normal flow of the contents of the intestine towards the anal canal.


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PMID (PMCID)
25560164
 MALE Infant, Newborn
Waardenburg syndrome presenting with constipation since birth.
Gupta R, Sharma SB, Mathur P, Agrawal LD.
Indian Pediatr. 2014;51(12):1013-4.
Suspect familial Shah-Waardenburg syndrome in a neonate of Waardenburg syndrome presenting with constipation since birth or intestinal obstruction.