Myectomy-myotomy for long segment Hirschsprung's disease in a patient with Haddad syndrome

被引：4
|
作者：
Otabor, Iyore A. [1 ]
Balint, Jane P. [2 ]
Besner, Gail E. [1 ]
机构：
[1] Ohio State Univ, Nationwide Childrens Hosp, Coll Med, Dept Pediat Surg, Columbus, OH 43205 USA
[2] Ohio State Univ, Nationwide Childrens Hosp, Coll Med, Dept Gastroenterol, Columbus, OH 43205 USA
来源：
JOURNAL OF PEDIATRIC SURGERY | 2009年 / 44卷 / 03期
关键词：
Hirschprung's disease; Ondine's curse; Haddad syndrome; TOTAL INTESTINAL AGANGLIONOSIS; HYPOVENTILATION SYNDROME;
D O I：
10.1016/j.jpedsurg.2008.10.115
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Hirschsprung's disease is a rare entity with an incidence of I in 5000 live born infants. Long segment Hirschsprung's disease occurs in approximately 5% to 10% of this patient population and is defined as a transition zone proximal to the sigmoid colon (Bodian M, Carter CO, Ward BC. Hirschsprung's disease. Lancet. 195 1; 1:302-309). The association of congenital central hypoventilation syndrome (also known as Ondine's curse) and Hirschsprung's disease is termed Haddad syndrome. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码：620 / 622
页数：3
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