Scalise Serena on Muck Rack

Scalise Serena

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Genetic Characterization and Multidisciplinary Management of Complete Androgen Insensitivity Syndrome: Unveiling a Novel AR Mutation

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By Di Chiara, Astorino Maria Francesca, Scalise Serena
| Wiley Online Library Verified
1 Introduction Androgen Insensitivity Syndrome (AIS) is a rare X-linked recessive disorder of sex development (DSD) [1, 2]. Population-based estimates suggest an overall AIS prevalence of approximately 4.1 per 100,000 individuals with a 46,Xy karyotype, whereas the incidence of complete AIS (CAIS) confirmed by molecular diagnosis has been reported between 1 in 20,400 and 1 in 99,100 genetic males [2].
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