Familial benign copper deficiency
id:
familial-benign-copper-deficiency-321-15145101
title:
Familial benign copper deficiency
text:
Familial benign copper deficiency, also known as Familial benign hypocupremia is a rare genetic disorder which is characterized by hypocupremia that causes symptoms such as epilepsy, hypotonia, seborrheic skin, thriving failure and mild anemia. Radiological findings include tibia and femur spurring. Transmission is thought to be either autosomal dominant or X-linked dominant. Symptoms are caused by a familial tendency of having low levels of copper within the body and can be improved with oral s
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Familial_benign_copper_deficiency
date created:
date modified:
2023-10-31T20:04:27Z
main entity:
{"identifier":"Q113380191","url":"https://www.wikidata.org/entity/Q113380191"}
image:
fields total:
13
integrity:
14