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Related Experiment Videos

Infantile XX male: a case report

A Miyashita, K Isurugi, H Aoki

    Clinical Genetics
    |October 1, 1976
    PubMed
    Summary

    This case study presents an infant with XX male syndrome, characterized by male external genitalia despite having XX chromosomes. Early diagnosis of this rare condition in infants is challenging.

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    Area of Science:

    • Genetics
    • Pediatrics
    • Endocrinology

    Background:

    • XX male syndrome is a rare genetic condition where individuals with XX chromosomes present with male phenotypes.
    • Infantile cases often pose diagnostic challenges due to ambiguous genitalia and the absence of typical Y chromosome markers.