Haddad Syndrome

Hellenic Journal of Cardiology - Tập 57 - Trang 45-47 - 2016
Alexander Tsoutsinos1, Evangelos Karanasios2, Andrew C. Chatzis3
1Department of Paediatric Cardiology, Onassis Cardiac Surgery Centre, Athens, Greece
2Department of Cardiology “Aghia Sophia” Children's Hospital, Athens, Greece
3Department of Paediatric and Congenital Cardiac Surgery, Onassis Cardiac Surgery Centre, Athens, Greece

Tài liệu tham khảo

Gronli, 2008, Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death, Pediatr Pulmonol, 43, 77, 10.1002/ppul.20744 Weese-Mayer, 2010, An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management, Am J Respir Crit Care Med, 181, 626, 10.1164/rccm.200807-1069ST Haddad, 1978, Congenital failure of automatic control of ventilation, gastrointestinal motility and heart rate, Medicine (Baltimore), 57, 517, 10.1097/00005792-197811000-00003 Silvestri, 2000, Cardiac rhythm disturbances among children with idiopathic congenital central hypoventilation syndrome, Pediatr Pulmonol, 29, 351, 10.1002/(SICI)1099-0496(200005)29:5<351::AID-PPUL3>3.0.CO;2-Z Gheissari, 1991, Transvenous pacemakers in children: relation of lead length to anticipated growth, Ann Thorac Surg, 52, 118, 10.1016/0003-4975(91)91431-T Nannapaneni, 2005, Retracing “Ondine's curse”, Neurosurgery, 57, 354, 10.1227/01.NEU.0000166684.69422.49 Trang, 2005, The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype, Chest, 127, 72, 10.1378/chest.127.1.72 Weese-Mayer, 1993 Axelrod, 2006, Pediatric autonomic disorders, Pediatrics, 118, 309, 10.1542/peds.2005-3032 van Limpt, 2004, The Phox2B homeobox gene is mutated in sporadic neuroblastomas, Oncogene, 23, 9280, 10.1038/sj.onc.1208157 Amiel, 2001, Hirschsprung disease, associated syndromes, and genetics: a review, J Med Genet, 38, 729, 10.1136/jmg.38.11.729 Garcia-Barceló, 2003, Association study of PHOX2B as a candidate gene for Hirschsprung's disease, Gut, 52, 563, 10.1136/gut.52.4.563 Jones, 2012, A triple threat: Down syndrome, congenital central hypoventilation syndrome, and Hirschsprung disease, Pediatrics, 130, e1382, 10.1542/peds.2011-3844 1999, Idiopathic congenital central hypoventilation syndrome: diagnosis and management. American Thoracic Society, Am J Respir Crit Care Med, 160, 368, 10.1164/ajrccm.160.1.16010 Fleming, 1980, Congenital central hypoventilation and sleep state, Pediatrics, 66, 425, 10.1542/peds.66.3.425 Shea, 1993, Ventilatory responses to exercise in humans lacking ventilatory chemo-sensitivity, J Physiol, 468, 623, 10.1113/jphysiol.1993.sp019792 Weese-Mayer, 2004, Genetics of congenital central hypoventilation syndrome: lessons from a seemingly orphan disease, Am J Respir Crit Care Med, 170, 16, 10.1164/rccm.200402-245PP Trang, 2005, Short-term blood pressure and heart rate variability in congenital central hypoventilation syndrome (Ondine's curse), Clin Sci (Lond), 108, 225, 10.1042/CS20040282 Rand, 2006, Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene, Am J Med Genet A, 140, 1687, 10.1002/ajmg.a.31336 Garrogue, 2002, Benefit of atrial pacing in sleep apnea syndrome, N Engl J Med, 346, 404, 10.1056/NEJMoa011919