A novel variant luteinizing hormone receptor in the first transmembrane helix of two homozygous Iranian patients: case report

Abstract Background Leydig cell hypoplasia (LCH) is a rare autosomal recessive endocrine syndrome that affects the normal development of male external genitalia in 46, XY individuals and is one of the causes of disorder of sexual differentiation (DSD) in males. The responsible gene of LCH is LHCGR w...

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Principais autores:	Samaneh Sharif, Saba Vakili, Moein Mobini, Malihe Lotfi, Fatemeh Zarei, Mohammad Reza Abbaszadegan, Rahim Vakili
Formato:	Artigo
Idioma:	Inglês
Publicado em:	SpringerOpen 2022-05-01
coleção:	Egyptian Journal of Medical Human Genetics
Assuntos:	Leydig cell hypoplasia Disorder of sexual differentiation LHCGR gene Novel variants
Acesso em linha:	https://doi.org/10.1186/s43042-022-00305-w
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