Sanjad–Sakati syndrome
id:
sanjad-sakati-syndrome-199-5486507
title:
Sanjad–Sakati syndrome
text:
Sanjad–Sakati syndrome is a rare autosomal recessive genetic condition seen in offspring of Middle Eastern origin. It was first described in Saudi Arabia, but has been seen in Qatari, Kuwaiti, Omani and other children from the Middle East as well as elsewhere. The condition is caused by mutations or deletions in the TBCE gene of Chromosome No.1. The condition is characterised by a triad of growth retardation and intellectual disability, hypoparathyroidism and dysmorphism.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Sanjad%E2%80%93Sakati_syndrome
date created:
date modified:
2024-03-04T02:26:53Z
main entity:
{"identifier":"Q21124512","url":"https://www.wikidata.org/entity/Q21124512"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/c/c8/Autorecessive_2.png","width":235,"height":275}
fields total:
13
integrity:
15