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Kallmann syndrome with a Tyr113His PROKR2 mutation
RATIONAL: Kallmann syndrome (KS) is a genetic gonadotropin-releasing hormone deficiency associated with hyposmia or anosmia and characterized by various modes of inheritance. PATIENT CONCERNS: A 16-year-old male did not reach puberty and was associated with hypogonadotropic hypogonadism and anosmia....
Gardado en:
| Publicado en: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Wolters Kluwer Health
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5585527/ https://ncbi.nlm.nih.gov/pubmed/28858133 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000007974 |
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