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Arquivos Brasileiros de Endocrinologia & Metabologia

versão impressa ISSN 0004-2730

Resumo

CORREA, Rafaela V. et al. Complete form of androgen insensitivity syndrome in brazilian patients due to P766A mutation in the androgen receptor. Arq Bras Endocrinol Metab [online]. 2005, vol.49, n.1, pp. 98-102. ISSN 0004-2730.  http://dx.doi.org/10.1590/S0004-27302005000100013.

Androgen insensitivity syndrome (AIS) is a rare X-linked disorder, caused by mutations in the androgen receptor gene (AR), associated with a variety of phenotypes in 46,XY individuals. We studied two 23 year-old twin-sisters with female social sex referred due to primary amenorrhea, who exhibited bilateral palpable gonads in the inguinal region and a 46,XY karyotype. The uterus was absent in pelvic sonograms. Basal LH levels were elevated (35 and 42U/L), with normal FSH (7.9 and 7.8U/L) and high testosterone levels (1330 and 1660ng/dl). The molecular analysis identified a missense mutation in exon 5 of AR gene that changed a proline to an alanine at position 766 of the protein. Proline 766 is a highly conserved amino acid in the AR of several species and is located in the androgen binding domain.

Palavras-chave : Androgen insensitivity syndrome (AIS); Androgen receptor (AR); Ambiguous genitalia; CAIS (Complete form of Androgen Insensitivity Syndrome); Male pseudohermaphroditism (MPH).

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