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Haddad syndrome

MONDO:0020493

Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease.

Also known as: Haddad syndrome, congenital central alveolar hypoventilation-Hirschsprung disease syndrome, ondine-Hirschsprung disease, ondine-Hirschsprung syndrome

3 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Digestive system disorder (160) Intestinal disorder (66) Human disease (14) Intestinal motility disease (9) Disease by body system or component (0)
Trials to join now! 2 Completed 1
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  • Kids' laxative study reveals how body handles the drug

    Knowledge-focused Completed

    This study measured levels of the laxative PEG 3350 and its breakdown products in the blood and urine of 158 children who were already taking it, compared to children not taking it. The goal was simply to learn how the body processes this medicine, not to change any treatments. R…

    Sponsor: Children's Hospital of Philadelphia • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:56 UTC

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