Fuqua-Berkovitz syndrome (Q100822): Difference between revisions

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Revision as of 17:35, 16 August 2026

Fuqua-Berkovitz syndrome is characterised by the association of ambiguous genitalia with well-developed Mullerian structures and testes with a normal appearance.
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ID_243268498
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    Fuqua-Berkovitz syndrome
    Fuqua-Berkovitz syndrome is characterised by the association of ambiguous genitalia with well-developed Mullerian structures and testes with a normal appearance.

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      CID11:ID_243268498
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      dki-india-ID_243268498
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      Concluído
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