Crandall syndrome
id:
crandall-syndrome-194-15734856
title:
Crandall syndrome
text:
Crandall syndrome is a very rare congenital disorder characterised by progressive sensorineural hearing loss, hair loss associated with pili torti, and hypogonadism demonstrated through low levels of luteinising hormone and growth hormone. It is thought to be an autosomal recessive disorder closely related to Björnstad syndrome which presents similarly but without hypogonadism. The condition was first reported by B. F. Crandall in 1973.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Crandall_syndrome
date created:
date modified:
2021-03-23T03:51:39Z
main entity:
{"identifier":"Q5181978","url":"https://www.wikidata.org/entity/Q5181978"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/f/f1/Autosomal_recessive_-_en.svg","width":738,"height":1283}
fields total:
13
integrity:
15