18p-
id:
18p-178-1013248
title:
18p-
text:
18p-, also known as monosomy 18p, deletion 18p syndrome, del(18p) syndrome, partial monosomy 18p, or de Grouchy syndrome 1, is a genetic condition caused by a deletion of all or part of the short arm of chromosome 18. It occurs in about 1 of every 50,000 births. Patients typically have petite frames, a short neck, and a distinctive stance. They may have mild microcephaly, a round, flat, expressionless face, a broad, flat nasal bridge, horizontal palpebral fissures, epicanthal folds, strabismus,
brand slug:
wiki
category slug:
encyclopedia
description:
Deletion of the short arm of chromosome 18
original url:
https://en.wikipedia.org/wiki/18p-
date created:
2008-08-12T22:31:57Z
date modified:
2024-09-04T06:25:20Z
main entity:
{"identifier":"Q4557543","url":"https://www.wikidata.org/entity/Q4557543"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/6/6d/Cebocephaly_%282%29.png","width":990,"height":990}
fields total:
13
integrity:
16