A Novel Mutation of Androgen Receptor Gene in Complete Androgen Insensitivity Syndrome
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چکیده
منابع مشابه
A Novel Mutation of Androgen Receptor Gene in Complete Androgen Insensitivity Syndrome
abdominal testes at the time of repair of bilateral inguinal hernia in infancy. At the age of 9 yr, the patient together with her mother visited our service to consult about the pathogenesis. The maternal uncle, reportedly, has “undervirilized external genitalia”. The mother declined to tell further family history. On examination, the patient’s height was 133.2 cm (≅25th percentile) and weight ...
متن کاملA novel mutation of the androgen receptor gene in familial complete androgen insensitivity syndrome.
OBJECTIVE Androgen insensitivity syndrome (AIS) is characterized by androgen receptor (AR) dysfunction. Its main characteristic is a female phenotype in an individual with a 46, XY karyotype. The molecular basis of this disorder was investigated in two individuals with familial AIS. PATIENTS AND METHODS The diagnoses of the two individuals were confirmed using ultrasonography, hormonal analys...
متن کاملNovel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome.
Mutations in the X-linked androgen receptor (AR) gene cause androgen insensitivity syndrome (AIS), resulting in an impaired embryonic sex differentiation in 46,XY genetic men. Complete androgen insensitivity (CAIS) produces a female external phenotype, whereas cases with partial androgen insensitivity (PAIS) have various ambiguities of the genitalia. Mild androgen insensitivity (MAIS) is charac...
متن کاملComplete 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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ژورنال
عنوان ژورنال: Clinical Pediatric Endocrinology
سال: 2007
ISSN: 0918-5739,1347-7358
DOI: 10.1297/cpe.16.59