Haddad syndrome (Q94162): Difference between revisions
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Síndrome de Haddad é um ytsnstorno genético congênito raro no qual a síndrome de hipoventilação central congênita (SHCC), ou síndrome de Ondine, ocorre simultaneamente com a doença de Hirschsprung. A aganglionose intestinal é mais extensa do que na doença de Hirschsprung clássica. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Haddad syndrome is a rare genetic congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Intestinal aganglionosis is more extensive than in classical Hirschsprung disease. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1685926536 / rank | |||||||||||||||
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CID11:ID_1685926536 | |||||||||||||||
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dki-india-ID_1685926536 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 09:17, 16 August 2026
Haddad syndrome is a rare genetic congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Intestinal aganglionosis is more extensive than in classical Hirschsprung disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1685926536 |
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| English | Haddad syndrome |
Haddad syndrome is a rare genetic congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Intestinal aganglionosis is more extensive than in classical Hirschsprung disease. |
Statements
CID11:ID_1685926536
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dki-india-ID_1685926536
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Concluído
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15 August 2026
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