Unraveling Delayed Puberty: A Rare Case of Congenital Hypogonadotropic Hypogonadism Masked by Celiac Disease and Plummer–Vinson Syndrome

ABSTRACT Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder that results in delayed puberty and infertility due to impaired secretion of gonadotropin‐releasing hormone (GnRH). Here, we present a case of a 25‐year‐old male with a known history of Plummer–Vinson syndrome and celiac dise...

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Bibliografiset tiedot

Päätekijät:	Osama Ahmad, Uzma Akbar, Fatima Sajjad, Muhammad Abdullah Ali, Umama Alam, Zaryab Bacha, Jibran Ikram, Malik W. Z. Khan
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Wiley 2025-10-01
Sarja:	Clinical Case Reports
Aiheet:	congenital hypogonadotropic hypogonadism functional hypogonadotropic hypogonadism genetic karyotyping Kallman syndrome
Linkit:	https://doi.org/10.1002/ccr3.70952
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