Crouzon syndrome
id:
crouzon-syndrome-198-15823034
title:
Crouzon syndrome
text:
Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial arch, which is the precursor of the maxilla and mandible. Because the branchial arches are important developmental features in a growing embryo, disturbances in their development create lasting and widespread effects. The syndrome is caused by a mutation in a gene on chromosome 10 that controls the body's production of fibroblast growth factor rec
brand slug:
wiki
category slug:
encyclopedia
description:
Genetic disorder of the skull and face
original url:
https://en.wikipedia.org/wiki/Crouzon_syndrome
date created:
date modified:
2024-03-30T15:14:38Z
main entity:
{"identifier":"Q779250","url":"https://www.wikidata.org/entity/Q779250"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/5/5c/Baby_with_Crouzon_Syndrome.jpg","width":569,"height":742}
fields total:
13
integrity:
15