Complete androgen insensitivity syndrome: A rare case report
Androgen receptor gene mutations on Xq12, which also have a 46XY karyotype abnormality, are the root cause of the X-linked uncommon recessive disorder of sex development known as androgen insensitivity syndrome (AIS). Complete AIS existed as a female, with normal breast, no uterus, ovaries, and fall...
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| Автори: | , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Wolters Kluwer Medknow Publications
2022-01-01
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| Серія: | National Journal of Clinical Anatomy |
| Предмети: | |
| Онлайн доступ: | http://www.njca.info/article.asp?issn=2277-4025;year=2022;volume=11;issue=4;spage=232;epage=235;aulast=Kambale |
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