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Title: Haddad syndrome. Author: Ławicka M, Sawicka J, Bąkowska G. Journal: Anaesthesiol Intensive Ther; 2013; 45(1):30-2. PubMed ID: 23572305. Abstract: Haddad syndrome is a rare genetically conditioned disease. We present a female newborn with congenital central hypoventilation syndrome associated with Hirschprung's disease. The infant is mechanically ventilated and parentally fed in a home setting. The diagnosis has been confirmed by the presence of 20/26 PHOX2B genetic mutation.[Abstract] [Full Text] [Related] [New Search]