Unverricht–Lundborg disease
id:
unverricht-lundborg-disease-206-3850231
title:
Unverricht–Lundborg disease
text:
Unverricht–Lundborg disease is the most common form of an uncommon group of genetic epilepsy disorders called the progressive myoclonus epilepsies. It is caused due to a mutation in the cystatin B gene (CSTB). The disease is named after Heinrich Unverricht, who first described it in 1891, and Herman Bernhard Lundborg, who researched it in greater detail in 1901 and 1903. ULD onsets in children between the ages of 6 and 16; there are no known cases in which the person was older than 18. Most case
brand slug:
wiki
category slug:
encyclopedia
description:
Genetic epilepsy disorder
original url:
https://en.wikipedia.org/wiki/Unverricht%E2%80%93Lundborg_disease
date created:
2006-10-24T14:15:09Z
date modified:
2024-09-10T14:12:53Z
main entity:
{"identifier":"Q2356131","url":"https://www.wikidata.org/entity/Q2356131"}
image:
fields total:
13
integrity:
15