| Literature DB >> 26023570 |
Sudipto Konar1, Debdeep Dasgupta2, Dipak Kumar Patra3, Angshuman De4, Barindranath Mallick5.
Abstract
The sufferers of complete androgen insensitivity syndrome (CAIS) are phenotypic females despite of having functional testes and normal male karyotype. They usually present late with primary amenorrhea but delayed diagnosis increases chance of gonadal malignancy. Alertness for this entity is crucial as with early diagnosis such disorder can be managed more appropriately for a better future. We hereby describe a case of CAIS in an 8-year-old girl presented with bilateral inguinal swellings. Endocrinological analysis, radiological investigations and cytogenetic studies were done. Investigations revealed absence of female internal genitalia. Karyotyping and molecular study confirmed the presence of Y chromosome. Parents were counseled regarding timely gonadectomy, fertility and other long term social issues.Entities:
Keywords: Gonadectomy; Karyotyping; Male pseudohermaphroditism
Year: 2015 PMID: 26023570 PMCID: PMC4437084 DOI: 10.7860/JCDR/2015/11411.5750
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X