Sialidosis
id:
sialidosis-204-6115078
title:
Sialidosis
text:
Mucolipidosis type I is an inherited lysosomal storage disease that results from a deficiency of the enzyme alpha-N -acetyl neuraminidase (sialidase). The lack of this enzyme results in an abnormal accumulation of complex carbohydrates known as mucopolysaccharides, and of fatty substances known as mucolipids. Both of these substances accumulate in bodily tissues.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Sialidosis
date created:
2005-08-27T22:37:53Z
date modified:
2024-09-09T22:08:12Z
main entity:
{"identifier":"Q7506658","url":"https://www.wikidata.org/entity/Q7506658"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/9/97/Sialic_acid.png","width":185,"height":80}
fields total:
13
integrity:
16