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  1. Da Aw L, Zain MM, Esteves SC, Humaidan P
    Int Braz J Urol, 2016 Nov-Dec;42(6):1237-1243.
    PMID: 27532119 DOI: 10.1590/S1677-5538.IBJU.2016.0225
    MAIN FINDINGS: A typical male looking adolescent with a legal female gender assignment presented with haematuria. Investigations led to the diagnosis of Persistent Mullerian Duct Syndrome. The condition is indeed a rare entity that needs a multidisciplinar team management. Case hypothesis: A case of Persistent Mullerian Duct Syndrome undiagnosed at birth because karyotyping was defaulted, thus resulting in a significant impact on the legal gender assignment and psychosocial aspects. Promising future implications: The reporting of this case is important to create awareness due to its rarity coupled with the rare presentation with hematuria as a possible masquerade to menstruation. There were not only medical implications, but also psychosocial and legal connotations requiring a holistic multidisciplinary management.
    Matched MeSH terms: 46, XY Disorders of Sex Development/diagnosis*
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