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SUN-204 Transient Hypergonadotropism Upon Pubertal Entry In A Boy With Delayed Puberty And A Heterozygous Mutation In TACR3

A boy presented with delayed puberty at age 13.5 years. His mother had idiopathic hypogonadotropic hypogonadism (IHH) with a heterozygous mutation in the gene TACR3 that the son had inherited. He had a normal sense of smell, no chronic diseases, and no use of medications. At his first physical exami...

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שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:J Endocr Soc
Main Authors: Barroso, Priscila, Seminara, Stephanie, Chan, Yee-Ming
פורמט: Artigo
שפה:Inglês
יצא לאור: Endocrine Society 2019
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC6553431/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-204
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