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Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita
X-linked adrenal hypoplasia congenita (AHC) is a rare disorder that usually presents clinically as adrenal insufficiency in early infancy. It is caused by mutations in the NR0B1 gene which is located on the short arm of chromosome X (Xp21). The NR0B1 gene plays an important role in normal developmen...
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| Publicado no: | Ann Pediatr Endocrinol Metab |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Society of Pediatric Endocrinology
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6177664/ https://ncbi.nlm.nih.gov/pubmed/30286574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2018.23.3.162 |
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