A rare case of Swyer syndrome from Pakistan in a young girl with primary amenorrhea and 46XY genotype
Swyer syndrome is a condition where individuals with a 46XY karyotype, typically associated with males, display complete gonadal dysgenesis and lack testicular differentiation. This results from a mutation in the SRY gene, which is essential for testis development. As a consequence, affected individ...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
SAGE Publishing
2023-11-01
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| Serija: | Women's Health |
| Online dostop: | https://doi.org/10.1177/17455057231213270 |
| Oznake: |
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