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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Dades bibliogràfiques
Publicat a:Ann Pediatr Endocrinol Metab
Autors principals: Serbis, Anastasios, Tsinopoulou, Vassiliki Regina, Mouzaki, Konstantina, Kotanidou, Eleni P., Giza, Styliani, Galli-Tsinopoulou, Assimina
Format: Artigo
Idioma:Inglês
Publicat: Korean Society of Pediatric Endocrinology 2018
Matèries:
Case Report
Accés en línia: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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