Distal spinal muscular atrophy type 2
id:
distal-spinal-muscular-atrophy-type-2-199-8166487
title:
Distal spinal muscular atrophy type 2
text:
Distal spinal muscular atrophy type 2 (DSMA2), also known as Jerash type distal hereditary motor neuropathy (HMNJ), is a very rare childhood-onset genetic disorder characterised by progressive muscle wasting affecting lower and subsequently upper limbs. The disorder has been described in Arab inhabitants of Jerash region in Jordan as well as in a Chinese family. The condition is linked to a genetic mutation in the SIGMAR1 gene on chromosome 19 and is likely inherited in an autosomal recessive ma
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Distal_spinal_muscular_atrophy_type_2
date created:
date modified:
2023-04-23T04:33:24Z
main entity:
{"identifier":"Q16944450","url":"https://www.wikidata.org/entity/Q16944450"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/f/f1/Autosomal_recessive_-_en.svg","width":738,"height":1283}
fields total:
13
integrity:
15