Spontaneous Improvement of Hypogonadotropic Hypogonadism in a Patient with <i>PCSK1</i> and <i>HS6ST1</i> Mutations: A Case Report

Spontaneous Improvement of Hypogonadotropic Hypogonadism in a Patient with <i>PCSK1</i> and <i>HS6ST1</i> Mutations: A Case Report

Kallmann syndrome (KS) is a form of hypogonadotropic hypogonadism (HH) characterized by gonadotropin-releasing hormone (GnRH) deficiency and anosmia due to defective neuronal migration. While traditionally considered irreversible, cases of spontaneous improvement of HH have been reported, suggesting...

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Main Authors:	Alanna Asgeirsson, Eujean Park, Vinicius Seidel, Mathew Shedd, Matheni Sathananthan, Tania Arous, Kevin Codorniz, Silvana Giannelli, Justin Do, Wyut Yi Thin, Arsenije Jelovac, Scott Lee
Format:	Article
Language:	English
Published:	MDPI AG 2025-07-01
Series:	Life
Subjects:	spontaneous hypogonadotropic hypogonadism reversal <i>PCSK1</i> mutation <i>HS6ST1</i> mutation GnRH neurons
Online Access:	https://www.mdpi.com/2075-1729/15/7/1151
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