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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...
Uloženo v:
| Vydáno v: | J Endocr Soc |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Endocrine Society
2019
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| Témata: | |
| On-line přístup: | 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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