Hecht Scott syndrome
id:
hecht-scott-syndrome-265-6507836
title:
Hecht Scott syndrome
text:
Hecht Scott syndrome is a rare genetic disease that causes congenital limb formation. The main characterisation is the aplasia or hypoplasia of bones of the limb. It is currently presenting in less than 1 in 1,000,000 newborns. It has been known to be more commonly present in males. It was first diagnosed in 2005 by Courtens et al. who recognised the malformations with his present case and four others that were similarly described in literature.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Hecht_Scott_syndrome
date created:
date modified:
2024-02-01T16:29:46Z
main entity:
{"identifier":"Q17254905","url":"https://www.wikidata.org/entity/Q17254905"}
image:
fields total:
13
integrity:
14