LMNA-related congenital muscular dystrophy
id:
lmna-related-congenital-muscular-dystrophy-304-12568288
title:
LMNA-related congenital muscular dystrophy
text:
Lamin A/C congenital muscular dystrophy (CMD) is a disease that it is included in laminopathies. Laminopathies are caused, among other mutations, to mutations in LMNA, a gene that synthesizes lamins A and C. Currently there are approximately 200 cases worldwide. This illness implies, like other muscular dystrophies, muscle weakness, motor difficulties and lack of control in the movement of the head, respiratory failure and cardiac abnormalities and symptoms are usually evident before the age of
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/LMNA-related_congenital_muscular_dystrophy
date created:
date modified:
2023-12-13T14:18:23Z
main entity:
{"identifier":"Q27835675","url":"https://www.wikidata.org/entity/Q27835675"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/4/4e/Autosomal_dominant_-_en.svg","width":738,"height":1260}
fields total:
13
integrity:
15