Meacham syndrome (Q94190): Difference between revisions

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Revision as of 09:19, 16 August 2026

Meacham syndrome is a multiple malformation syndrome characterised by congenital diaphragmatic abnormalities, genital defects (true double vagina or septate vagina, absent uterus, abnormal male gonads in the presence of normal external female genitalia or male pseudohermaphroditism with abnormal internal female genitalia) and complex cyanotic congenital heart defects.
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    Meacham syndrome
    Meacham syndrome is a multiple malformation syndrome characterised by congenital diaphragmatic abnormalities, genital defects (true double vagina or septate vagina, absent uterus, abnormal male gonads in the presence of normal external female genitalia or male pseudohermaphroditism with abnormal internal female genitalia) and complex cyanotic congenital heart defects.

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      CID11:ID_1307620543
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