Defects in GnRH Neuron Migration/Development and Hypothalamic-Pituitary Signaling Impact Clinical Variability of Kallmann Syndrome

Kallmann syndrome (KS) is a combination of isolated hypogonadotropic hypogonadism (IHH) with olfactory dysfunction, representing a heterogeneous disorder with a broad phenotypic spectrum. The genetic background of KS has not yet been fully established. This study was conducted on 46 Polish KS subjec...

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Publicado en:Genes (Basel)
Autores principales: Kałużna, Małgorzata, Budny, Bartłomiej, Rabijewski, Michał, Kałużny, Jarosław, Dubiel, Agnieszka, Trofimiuk-Müldner, Małgorzata, Wrotkowska, Elżbieta, Hubalewska-Dydejczyk, Alicja, Ruchała, Marek, Ziemnicka, Katarzyna
Formato: Artigo
Lenguaje:Inglês
Publicado: MDPI 2021
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC8229512/
https://ncbi.nlm.nih.gov/pubmed/34198905
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12060868
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