Genetic Analysis of Patients with Congenital Hypogonadotropic Hypogonadism: A Case Series

Congenital hypogonadotropic hypogonadism (cHH)/Kallmann syndrome (KS) is a rare genetic disorder with variable penetrance and a complex inheritance pattern. Consequently, it does not always follow Mendelian laws. More recently, digenic and oligogenic transmission has been recognized in 1.5–15% of ca...

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Detalles Bibliográficos
Autores principales: Cannarella, Rossella, Gusmano, Carmelo, Condorelli, Rosita A., Bernini, Andrea, Kaftalli, Jurgen, Maltese, Paolo Enrico, Paolacci, Stefano, Dautaj, Astrit, Marceddu, Giuseppe, Bertelli, Matteo, La Vignera, Sandro, Calogero, Aldo E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138801/
https://www.ncbi.nlm.nih.gov/pubmed/37108593
http://dx.doi.org/10.3390/ijms24087428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138801/
https://www.ncbi.nlm.nih.gov/pubmed/37108593
http://dx.doi.org/10.3390/ijms24087428

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