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Genetics of Idiopathic Hypogonadotropic Hypogonadism

Idiopathic hypogonadotropic hypogonadism (IHH) comprises a group of disorders characterized by deficient secretion or action of gonadotropin-releasing hormone (GnRH), leading to impaired pubertal development and infertility. Traditionally, IHH is classified into Kallmann syndrome, associated with an...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: A. Kemal Topaloğlu, Leman Damla Kotan
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Pediatric Endocrinology and Diabetes Society 2026-06-01
Sarja:JCRPE
Aiheet:
Linkit:https://www.jcrpe.org/articles/genetics-of-idiopathic-hypogonadotropic-hypogonadism/doi/jcrpe.galenos.2025.2025-6-23
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