Exon 1 deletion of the androgen receptor gene causing complete androgen insensitivity syndrome in a newborn: a case report
ObjectiveTo genetically characterize a case of neonatal complete androgen insensitivity syndrome (CAIS) and identify the underlying molecular defect.MethodsThis was a retrospective analysis of the clinical data, diagnosis, and treatment of a case of CAIS in the Second Hospital of Lanzhou University....
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2025-04-01
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| Serie: | Frontiers in Pediatrics |
| Soggetti: | |
| Accesso online: | https://www.frontiersin.org/articles/10.3389/fped.2025.1508618/full |
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