ONDINE-HIRSCHSPRUNG SYNDROME (HADDAD SYNDROME) - FURTHER DELINEATION IN 2 CASES AND REVIEW OF THE LITERATURE

被引:48
作者
VERLOES, A
ELMER, C
LACOMBE, D
HEINRICHS, C
REBUFFAT, E
DEMARQUEZ, JL
MONCLA, A
ADAM, E
机构
[1] CHILDREN HOSP,PAEDIAT & MED GENET CLIN,BORDEAUX,FRANCE
[2] REINE FABIOLA UNIV HOSP CHILDREN,BRUSSELS,BELGIUM
[3] LA TIMONE HOSP,CTR GENET,MARSEILLE,FRANCE
[4] UNIV HOSP TIVOLI,NEONATAL INTENS CARE UNIT,LA LOUVIERE,BELGIUM
[5] FREE UNIV BRUSSELS,CTR HUMAN GENET,B-1050 BRUSSELS,BELGIUM
[6] CHILDREN HOSP,PAEDIAT INTENS CARE UNIT,BORDEAUX,FRANCE
关键词
HIRSCHSPRUNG DISEASE; NEUROCHRISTOPATHY; ONDINES CURSE; REVIEW;
D O I
10.1007/BF02072522
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Two unrelated children with congenital central hypoventilation syndrome (CCHS-Ondine syndrome) and long segment Hirschsprung disease are reported. Patient 1, a girl, is still alive at 3 years. Patient 2, a boy, died of viral pneumonia at 5.5 years. Continuous mechanical ventilation was necessary for months and those children could never be weaned from the respirator during sleep. Seventeen cases of this complex neurocristopathy are reviewed. Only six children (including our cases) survived beyond 2 years of age. Hypotonia, delay in developmental milestones or epilepsy were frequently observed. Ventilator dependency does not improve with time. Multifocal congenital neuroblastoma occurred in two children. Aetiology is unknown.
引用
收藏
页码:75 / 77
页数:3
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