Erythrokeratodermia variabilis
id:
erythrokeratodermia-variabilis-284-4612730
title:
Erythrokeratodermia variabilis
text:
Erythrokeratodermia variabilis is a rare autosomal dominant disorder that usually presents at birth or during the first year of life. To date, it is thought to be caused by mutations in genes encoding for connexin channels proteins in the epidermis, leading to the misregulation of homeostasis in keratinocytes. One type is characterized by generalized, persistent, brown hyperkeratosis with accentuated skin markings, while a second type is localized, with involvement that is limited in extent and
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Erythrokeratodermia_variabilis
date created:
date modified:
2022-05-25T23:59:51Z
main entity:
{"identifier":"Q3591493","url":"https://www.wikidata.org/entity/Q3591493"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/4/4e/Autosomal_dominant_-_en.svg","width":738,"height":1260}
fields total:
13
integrity:
15