KBG syndrome
id:
kbg-syndrome-290-6668707
title:
KBG syndrome
text:
KBG syndrome is a rare genetic disease that is the result of a mutation in the ANKRD11 gene at location 16q24.3. Only about a hundred known cases have been reported, although it is expected to be under-reported. The syndrome was first described by Herrmann in 1975 in three distinct families. Herrmann proposed the name KBG syndrome after the initials of affected families' last names, which aren't known to the general public.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/KBG_syndrome
date created:
date modified:
2023-12-02T23:57:33Z
main entity:
{"identifier":"Q1718432","url":"https://www.wikidata.org/entity/Q1718432"}
image:
fields total:
13
integrity:
14