Camurati–Engelmann disease
id:
camurati-engelmann-disease-172-13618515
title:
Camurati–Engelmann disease
text:
Camurati–Engelmann disease (CED) is a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton. It is also known as progressive diaphyseal dysplasia. It is a form of dysplasia. Patients typically have heavily thickened bones, especially along the shafts of the long bones. The skull bones may be thickened so that the passages through the skull that carry nerves and blood vessels become narrowed, possibly leading to sensory deficits, blindness, or deafness
brand slug:
wiki
category slug:
encyclopedia
description:
Rare skeletal genetic disorder
original url:
https://en.wikipedia.org/wiki/Camurati%E2%80%93Engelmann_disease
date created:
2008-02-29T14:04:42Z
date modified:
2024-09-02T00:06:08Z
main entity:
{"identifier":"Q498487","url":"https://www.wikidata.org/entity/Q498487"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/4/4e/Autosomal_dominant_-_en.svg","width":738,"height":1260}
fields total:
13
integrity:
16