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...

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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

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