A case of mild partial androgen insensitivity syndrome in a juvenile boy
Androgen insensitivity syndrome (AIS) is a rare disorder with X-linked recessive inheritance in 46 XY patients. The clinical manifestations vary between patients, especially regarding external genitalia development. Herein, the case of AIS in a 13-year-old male, who was born with hypospadias and pre...
| Główni autorzy: | , , , |
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| Format: | Artykuł |
| Język: | English |
| Wydane: |
SAGE Publishing
2024-03-01
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| Seria: | Journal of International Medical Research |
| Dostęp online: | https://doi.org/10.1177/03000605241232520 |