Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes
Purpose Androgen insensitivity syndrome (AIS) is a rare X-linked recessive disorder caused by unresponsiveness to androgens because of mutations in the AR gene. Here, we investigated the clinical outcomes and molecular spectrum of AR variants in patients with AIS attending a single academic center....
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Korean Society of Pediatric Endocrinology
2023-09-01
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Series: | Annals of Pediatric Endocrinology & Metabolism |
Subjects: | |
Online Access: | http://e-apem.org/upload/pdf/apem-2244152-076.pdf |