Waardenburg syndrome type 1
id:
waardenburg-syndrome-type-1-268-12025943
title:
Waardenburg syndrome type 1
text:
Waardenburg syndrome type 1 is a congenital disorder that caused by a mutation in the PAX3 gene that results in abnormal development in the neural crest during early development. Type 1 results in early graying and white forelock and a notable distance between the eyes, noted as dystopia canthorum. Common symptoms of the disease also includes non-progressive hearing loss in majority of patients with type 1. Patients can display complete or partial heterochromia and hypoplastic blue irides and co
brand slug:
wiki
category slug:
encyclopedia
description:
Congenital disorder
original url:
https://en.wikipedia.org/wiki/Waardenburg_syndrome_type_1
date created:
date modified:
2024-02-15T20:49:20Z
main entity:
{"identifier":"Q3508711","url":"https://www.wikidata.org/entity/Q3508711"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/a/a2/Waardenburg_syndrome.jpg","width":688,"height":1020}
fields total:
13
integrity:
15