Meacham syndrome (Q94190): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1307620543 / rank
 
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CID11:ID_1307620543
Property / CURIE: CID11:ID_1307620543 / rank
 
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dki-india-ID_1307620543
Property / Canary Token: dki-india-ID_1307620543 / rank
 
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
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CalendarGregorian
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Property / Collection date: 15 August 2026 / rank
 
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Latest 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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ID_1307620543
    English
    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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      dki-india-ID_1307620543
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      Concluído
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      15 August 2026
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