Keppen–Lubinsky syndrome
id:
keppen-lubinsky-syndrome-194-16131657
title:
Keppen–Lubinsky syndrome
text:
Keppen–Lubinsky syndrome is an extremely rare congenital disorder. The minimal clinical criteria for the Keppen–Lubinsky syndrome are as follows: normal growth parameters at birth, postnatal growth failure, peculiar face with an aged appearance, skin tightly adherent to facial bones, generalized lipodystrophy, microcephaly, and development delay. Keppen-Lubinsky syndrome is caused by mutation in the inwardly rectifying K+ channels encoded by KCNJ6 gene.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Keppen%E2%80%93Lubinsky_syndrome
date created:
date modified:
2023-11-17T09:16:07Z
main entity:
{"identifier":"Q3961676","url":"https://www.wikidata.org/entity/Q3961676"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/4/4e/Autosomal_dominant_-_en.svg","width":738,"height":1260}
fields total:
13
integrity:
15