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. | |||
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 |
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| 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. |
