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Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism
Neonatal micropenis and cryptorchidism raise the suspicion of congenital hypogonadotropic hypogonadism (CHH), a rare genetic disorder caused by GnRH deficiency. Low plasma testosterone levels and low gonadotropins during minipuberty provide a clinical diagnostic clue, yet these tests are seldomly pe...
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| Publicat a: | Clin Genet |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5513751/ https://ncbi.nlm.nih.gov/pubmed/28195315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12996 |
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