Holmes-Schepens syndrome (Q94179): Difference between revisions

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Síndrome de Holmes-Schepens, também conhecida como síndrome de Donnai-Barrow, é uma síndrome de malformação caracterizada por hérnia diafragmática, exonfalo, hipertelorismo, agenesia do corpo caloso, surdez neurossensorial grave e miopia grave.
description / endescription / en
 
Holmes-Schepens syndrome also known as Donnai-Barrow syndrome is a malformation syndrome characterised by diaphragmatic hernia, exomphalos, hypertelorism, agenesis of the corpus callosum, severe sensorineural deafness, and severe myopia.
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Property / Canonical URI: https://id.who.int/icd/entity/1171547698 / rank
 
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CID11:ID_1171547698
Property / CURIE: CID11:ID_1171547698 / rank
 
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dki-india-ID_1171547698
Property / Canary Token: dki-india-ID_1171547698 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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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
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 09:18, 16 August 2026

Holmes-Schepens syndrome also known as Donnai-Barrow syndrome is a malformation syndrome characterised by diaphragmatic hernia, exomphalos, hypertelorism, agenesis of the corpus callosum, severe sensorineural deafness, and severe myopia.
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ID_1171547698
    English
    Holmes-Schepens syndrome
    Holmes-Schepens syndrome also known as Donnai-Barrow syndrome is a malformation syndrome characterised by diaphragmatic hernia, exomphalos, hypertelorism, agenesis of the corpus callosum, severe sensorineural deafness, and severe myopia.

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      CID11:ID_1171547698
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      dki-india-ID_1171547698
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      Concluído
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      15 August 2026
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