Different Clinical Presentations and Management in Complete Androgen Insensitivity Syndrome (CAIS)

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Complete Androgen Insensitivity Syndrome.

The incidence of Complete Androgen Insensitivity Syndrome (CAIS) is about 1 in 20,000. People with CAIS are normal appearing females, despite the presence of testes and a 46, XY chromosome constitution. We came across a case in which a 17 years old girl presented with the complaint of inguinal hernia and amenorrhea. Subsequent investigations were done revealing absence of female internal genita...

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[Complete androgen insensitivity syndrome: diagnosis and clinical characteristics].

Complete androgen insensitivity syndrome (CAIS) is a genetic disease caused by mutations in the androgen receptor gene. CAIS patients are individuals with a 46, XY karyotype. The phenotype consists in female external genitalia, short vagina, absent mullerian structures, and abdominal, inguinal or intralabial testes. Our aim is to describe a group of CAIS patients in our centre and identify the ...

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Comment on “Complete Androgen Insensitivity Syndrome: Optimizing Diagnosis and Management”

1 Department of Medical and Surgical Sciences, Pediatric Unit, Program of Endocrinology, University of Bologna, Italy 2 Department of Obstetrics and Gynecology, University of Bologna, Italy 3 Adolescent Medicine, Department of Obstetrics, Gynecology and Pediatrics, University Hospital, Pisa, Italy 4Clinical Psychology Unit, Department of Pediatrics, University of Bologna, Italy 5 Pediatric Surg...

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ژورنال

عنوان ژورنال: International Journal of Environmental Research and Public Health

سال: 2019

ISSN: 1660-4601

DOI: 10.3390/ijerph16071268