UnknownNot Applicable

PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood

Taiwan20 participantsStarted 2009-09

Plain-language summary

Detect the PHOX2B Mutation-confirmed congenital central hypoventilation syndrome

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Members of familiar congenital central hypoventilation syndrome Exclusion Criteria: * Refuse to participate study

respiratory failure

Timeframe: cross sectional observation

NCT IDNCT00652964

SponsorNational Taiwan University Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2012-12

Peilin Lee, M.D.