46 XY undervirulized male DSD: Reporting a patient with prenatally diagnosed disorder/difference of sex development (DSD) with heterozygous LHCGR mutations

Leydig cell hypoplasia is a rare autosomal recessive condition caused by mutations in luteinizing hormone/chorionic gonadotropin receptor (LHCGR) genes in which 46, XY patients demonstrate a wide spectrum of disorders/differences of sex development (DSD) phenotypes ranging from normal female externa...

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Detalles Bibliográficos
Autores principales: Fendereski, Kiarad, Carey, John, Timme, Kathleen, Hayes, Katherine, Robnett, Jessica, Schaeffer, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671494/
https://www.ncbi.nlm.nih.gov/pubmed/34950567
http://dx.doi.org/10.1016/j.eucr.2021.101971

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671494/
https://www.ncbi.nlm.nih.gov/pubmed/34950567
http://dx.doi.org/10.1016/j.eucr.2021.101971

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