Duarte galactosemia
id:
duarte-galactosemia-311-7549309
title:
Duarte galactosemia
text:
Duarte galactosemia is an inherited condition associated with diminished ability to metabolize galactose due to a partial deficiency of the enzyme galactose-1-phosphate uridylyltransferase. DG differs from classic galactosemia in that patients with Duarte galactosemia have partial GALT deficiency whereas patients with classic galactosemia have complete, or almost complete, GALT deficiency. Duarte galactosemia (DG) is much more common than classic galactosemia, and is estimated to affect close to
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Duarte_galactosemia
date created:
date modified:
2023-10-27T15:31:22Z
main entity:
{"identifier":"Q25323784","url":"https://www.wikidata.org/entity/Q25323784"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/2/2d/Leloir_pathway_cropped.jpg","width":579,"height":378}
fields total:
13
integrity:
15