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Article type: Research Article
Authors: Jaiyeola, P.* | El-Metwally, D. | Viscardi, R. | Greene, C. | Woo, H.
Affiliations: Department of Pediatrics, University of Maryland Medical Center, Baltimore, MD, USA
Correspondence: [*] Corresponding author: Patti Jo Jaiyeola, M.D., University of Maryland Medical Center, Department of Pediatrics, 22 South Greene Street, N5W70, Baltimore, MD 21201, USA. Tel.: +1 410 328 6662; Fax: +1 410 328 0646; pjaiyeola@umm.edu
Abstract: Congenital central hypoventilation syndrome (CCHS) is an uncommon cause of apnea in the newborn characterized by the occurrence of apnea predominantly during sleep. Haddad syndrome is CCHS with Hirschsprung’s disease. We report a newborn with Haddad syndrome that had a family history of spinal muscular atrophy and discuss aspects of CCHS and important considerations in the evaluation of apnea in the term newborn.
Keywords: Haddad syndrome, congenital hypoventilation syndrome, Hirschsprung’s disease
DOI: 10.3233/NPM-15814058
Journal: Journal of Neonatal-Perinatal Medicine, vol. 8, no. 2, pp. 165-168, 2015
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