Waardenburg syndrome type 4A
id:
waardenburg-syndrome-type-4a-269-1669555
title:
Waardenburg syndrome type 4A
text:
Waardenburg syndrome type 4A is an extremely rare congenital disorder caused by a mutation in an endothelin receptor gene. It results in common Waardenburg syndrome symptoms such as abnormal hair and skin pigmentation and heterochromia, but also present with symptoms of Hirschsprung's disease. Symptoms include abdominal pain and bowel obstruction. Waardenburg syndrome type 4A is the rarest among the types, appearing only once in about every 1,000,000 individuals. There have only been a total of
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Waardenburg_syndrome_type_4A
date created:
date modified:
2024-02-15T20:51:49Z
main entity:
{"identifier":"Q32145171","url":"https://www.wikidata.org/entity/Q32145171"}
image:
fields total:
13
integrity:
14