Kallmann Syndrome Due to Heterozygous Mutation in SOX10 Coexisting With Waardenburg Syndrome Type II: Case Report and Review of Literature

Kallmann Syndrome Due to Heterozygous Mutation in SOX10 Coexisting With Waardenburg Syndrome Type II: Case Report and Review of Literature

IntroductionKallmann syndrome (KS) is idiopathic hypogonadotropic hypogonadism with olfactory loss or decline. Waardenburg syndrome type II (WS2) is a clinically and genetically heterogeneous disease, characterized by congenital sensorineural deafness and abnormal pigmentation of the iris, hair, and...

Full description

Bibliographic Details
Main Authors: Kan Chen, Haoyu Wang, Yaxin Lai
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Endocrinology
Subjects:
Kallmann syndrome
Waardenburg syndrome type Ⅱ
SOX10 mutations
sensorineural deafness
hypogonadotropic hypogonadism
co-occurrence
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2020.592831/full

Internet

https://www.frontiersin.org/articles/10.3389/fendo.2020.592831/full

Similar Items