- Haddad Syndrome with PHOX2B Gene Mutation in a Korean Infant
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Lee CW, Lee JH, Jung EY, Choi SO, Kim CS, Lee SL, Kim DK
- KMID: 1782126
- J Korean Med Sci.
- 2011 Feb;26(2):312-315.
- doi: 10.3346/jkms.2011.26.2.312
Congenital central hypoventilation syndrome with Hirschsprung's disease, also known as Haddad syndrome, is an extremely rare disorder with variable symptoms. Recent studies described that congenital central hypoventilation syndrome had deep... -
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