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SUN-LB15 A Case of Familial Male-Limited Precocious Puberty With a Novel Mutation

Introduction: Familial Male-Limited Precocious Puberty (FMPP), also known as testotoxicosis, is a rare cause of precocious puberty in males. It is caused by a mutation in the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) gene, resulting in the receptor to be constitutively activated. T...

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Argitaratua izan da:J Endocr Soc
Egile Nagusiak: Owens, Lindsey L, Carakushansky, Mauri, Gurnurkar, Shilpa
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2020
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208815/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.2065
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