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Results 1 - 3 of 3 for Central hypoventilation "syndrome," "congenital," 3
  1. Congenital central hypoventilation syndrome 
    ... Yen S, Kun SS, Keens TG, Perez IA. Three-Generation Family With Congenital Central Hypoventilation Syndrome and Novel PHOX2B Gene Non-Polyalanine Repeat Mutation. ...
    https://medlineplus.gov/...ngenital-central-hypoventilation-syndrome - Genetics
  2. PHOX2B gene 
    ... EM, Zhou L, Rand CM, Weese-Mayer DE. Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype. Am J Respir Crit Care Med. 2006 Nov 15;174(10):1139-44. doi: 10.1164/rccm.200602-305OC. Epub 2006 Aug 3. Citation on PubMed Di Lascio S, Benfante R, ...
    https://medlineplus.gov/genetics/gene/phox2b - Genetics
  3. Hirschsprung disease 
    ... Waardenburg syndrome, type IV; Mowat-Wilson syndrome; or congenital central hypoventilation syndrome. These cases are described as syndromic. Hirschsprung disease ...
    https://medlineplus.gov/genetics/condition/hirschsprung-disease - Genetics