Okamoto syndrome
id:
okamoto-syndrome-309-15250888
title:
Okamoto syndrome
text:
Okamoto syndrome (OS), also known as Au–Kline syndrome (AKS), is a very rare autosomal dominant genetic condition characterised by congenital hydronephrosis, low muscle tone, heart defects, intellectual disability and characteristic facial features. Those affected often have neurological and skeletal abnormalities, as well as frequent urinary tract infections. Language and walking are usually delayed. Facial features include prominent, downturned ears, an open, downturned mouth and drooping eyel
brand slug:
wiki
category slug:
encyclopedia
description:
Rare genetic condition involving urinary, heart, facial and neurological features
original url:
https://en.wikipedia.org/wiki/Okamoto_syndrome
date created:
date modified:
2023-10-27T14:00:46Z
main entity:
{"identifier":"Q55783391","url":"https://www.wikidata.org/entity/Q55783391"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/a/a1/Okamoto_syndrome.png","width":647,"height":741}
fields total:
13
integrity:
15