{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,3,30]],"date-time":"2022-03-30T12:04:06Z","timestamp":1648641846538},"reference-count":11,"publisher":"Springer Publishing Company","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neonatal Network"],"published-print":{"date-parts":[[2005,7]]},"abstract":"<jats:p>Hirschsprung\u2019s disease (HD), also known as congenital aganglionic megacolon, is a relatively common cause of congenital obstruction of the colon. Congenital central hypoventilation syndrome (CCHS), also known as Ondine\u2019s curse, is a rare condition involving failed autonomic respiration in the absence of cardiorespiratory disease resulting in inadequate alveolar ventilation. Both conditions typically present in the newborn period and belong to a group of disorders referred to as neurocristopathies.<\/jats:p><jats:p>HD and CCHS most commonly exist as discrete entities, but the coexistence of them is now called Haddad syndrome. Although few documented cases of Haddad syndrome exist in the literature, the association of CCHS and HD suggests a common etiology involving neural crest development.<\/jats:p>","DOI":"10.1891\/0730-0832.24.4.41","type":"journal-article","created":{"date-parts":[[2011,11,16]],"date-time":"2011-11-16T14:27:34Z","timestamp":1321453654000},"page":"41-44","source":"Crossref","is-referenced-by-count":2,"title":["Haddad Syndrome: A Case Study"],"prefix":"10.1891","volume":"24","author":[{"given":"Lisa","family":"Shuman","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Diane","family":"Youmans","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"793","published-online":{"date-parts":[[2005,7,1]]},"reference":[{"issue":"1","key":"1","doi-asserted-by":"crossref","first-page":"74","DOI":"10.1097\/00001574-200201000-00013","article-title":"The pathogenesis of Hirschsprung's disease.","volume":"18","author":"WM. Belknap","year":"2002","journal-title":"Current Opinion in Gastroenterology"},{"issue":"10","key":"2","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1006\/dbio.1998.8876","article-title":"GDNF and ET-3 differentially modulate the numbers of avian enteric neural crest cells and enteric neurons in vitro.","volume":"197","author":"CJ Hearn","year":"1998","journal-title":"Developmental Biology"},{"key":"3","unstructured":"Ross AJ. 1998. Organogenesis, innervation, and histologic development of the gastrointestinal tract. In <i>Fetal and Neonatal Physiology<\/i>, 2nd ed., Polin RA, and Fox WW, eds. Philadelphia: WB Saunders, 1342\u20131353."},{"issue":"1","key":"4","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1164\/ajrccm.160.1.16010","article-title":"Idiopathic congenital central hypoventilation syndrome.","volume":"160","author":"Society. 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Ontario: BC Deker, 237\u2013259."},{"issue":"4","key":"7","doi-asserted-by":"crossref","first-page":"316","DOI":"10.1136\/adc.78.4.316","article-title":"Congenital central hypoventilation syndrome and Hirschsprung's disease.","volume":"78","author":"GD Croaker","year":"1998","journal-title":"Archives of Disease in Childhood"},{"key":"8","unstructured":"Fontan JJP, and Haddad GG. 2000. Respiratory pathophysiology. In <i>Nelson Textbook of Pediatrics<\/i>, 16th ed., Behrman RE, Kliegman RM, and Jenson HB, eds. Philadelphia: WB Saunders, 1241\u20131252."},{"issue":"6","key":"9","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1097\/00063198-199911000-00002","article-title":"Novel insights into congenital hypoventilation syndrome.","volume":"5","author":"D Gozal","year":"1999","journal-title":"Current Opinion in Pulmonary Medicine"},{"issue":"6","key":"10","doi-asserted-by":"crossref","first-page":"517","DOI":"10.1097\/00005792-197811000-00003","article-title":"Congenital failure of autonomic control of ventilation, gastrointestinal motility and heart rate.","volume":"57","author":"GG Haddad","year":"1978","journal-title":"Medicine"},{"key":"11","doi-asserted-by":"crossref","unstructured":"American Academy of Pediatrics. 1998. Policy statement: Hospital discharge of the high-risk neonate<i>\u2013<\/i>proposed guidelines. Retrieved December 28, 2004, from <a target=\"_blank\" href='http:\/\/aappolicy.aappublications.org\/cgi\/content\/full\/pediatrics;102\/2\/411?fulltext=hospital+discharge&searchid=QID_NOT_SET'>http:\/\/aappolicy. aappublications.org\/cgi\/content\/full\/pediatrics;102\/2\/ 411?fulltext=hospital+discharge&searchid=QID_NOT_SET<\/a>","DOI":"10.1542\/peds.102.2.411"}],"container-title":["Neonatal Network"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1891\/0730-0832.24.4.41","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,9,18]],"date-time":"2019-09-18T21:45:16Z","timestamp":1568843116000},"score":1,"resource":{"primary":{"URL":"http:\/\/connect.springerpub.com\/lookup\/doi\/10.1891\/0730-0832.24.4.41"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,7]]},"references-count":11,"journal-issue":{"issue":"4","published-online":{"date-parts":[[2005,7,1]]},"published-print":{"date-parts":[[2005,7]]}},"alternative-id":["10.1891\/0730-0832.24.4.41"],"URL":"https:\/\/doi.org\/10.1891\/0730-0832.24.4.41","relation":{},"ISSN":["0730-0832","1539-2880"],"issn-type":[{"value":"0730-0832","type":"print"},{"value":"1539-2880","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,7]]}}}