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...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Korean Society of Pediatric Endocrinology
2018-09-01
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Series: | Annals of Pediatric Endocrinology & Metabolism |
Subjects: | |
Online Access: | http://e-apem.org/upload/pdf/apem-2018-23-3-162.pdf |