X-linked spinal muscular atrophy type 2
id:
x-linked-spinal-muscular-atrophy-type-2-282-16595618
title:
X-linked spinal muscular atrophy type 2
text:
X-linked spinal muscular atrophy type 2, also known as arthrogryposis multiplex congenita X-linked type 1 (AMCX1), is a rare neurological disorder involving death of motor neurons in the anterior horn of spinal cord resulting in generalised muscle wasting (atrophy). The disease is caused by a mutation in UBA1 gene and is passed in an X-linked recessive manner by carrier mothers to affected sons. Affected babies have general muscle weakness, weak cry and floppy limbs; consequently, the condition
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/X-linked_spinal_muscular_atrophy_type_2
date created:
date modified:
2023-12-27T01:57:16Z
main entity:
{"identifier":"Q8041562","url":"https://www.wikidata.org/entity/Q8041562"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/c/c7/X-linked_recessive.svg","width":600,"height":911}
fields total:
13
integrity:
15