Ghosal hematodiaphyseal dysplasia
id:
ghosal-hematodiaphyseal-dysplasia-200-9451161
title:
Ghosal hematodiaphyseal dysplasia
text:
Ghosal hematodiaphyseal dysplasia, is a rare, autosomal recessive disease, characterized by diaphyseal dysplasia and metaphyseal dysplasia of the long bones and refractory anemia. It is associated with a deficiency of Thromboxane-A synthase, which produces Thromboxane A2. Although this disease is like Camurati–Engelmann disease where there is also diaphyseal dysplasia, there are, however, reasons to differentiate between the two diseases. As mentioned earlier, both diseases affect diaphysis, but
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Ghosal_hematodiaphyseal_dysplasia
date created:
date modified:
2022-07-24T02:38:39Z
main entity:
{"identifier":"Q5556985","url":"https://www.wikidata.org/entity/Q5556985"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/0/09/Thromboxane_A2_acsv.svg","width":1350,"height":964}
fields total:
13
integrity:
15