CONGENITAL DIAPHRAGMATIC-HERNIA ASSOCIATED WITH IPSILATERAL UPPER LIMB REDUCTION DEFECTS - REPORT OF A CASE WITH THUMB HYPOPLASIA

被引:11
|
作者
LERONE, M
SOLIANI, M
COREA, D
ROMEO, G
MARTUCCIELLO, G
SILENGO, MC [1 ]
机构
[1] UNIV TORINO,IST DISCIPLINE PEDIAT,PIAZZA POLONIA 94,I-10134 TURIN,ITALY
[2] IST GIANNINA GASLINI,DIV CHIRURG,I-16148 GENOA,ITALY
[3] IST GIANNINA GASLINI,UNITA TERAPIA INTENS,I-16148 GENOA,ITALY
[4] IST GIANNINA GASLINI,AMBULATORIO GENET MOLEC,I-16148 GENOA,ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 44卷 / 06期
关键词
BOCHDALEK DIAPHRAGMATIC HERNIA; CERVICAL NEURAL CREST; MALFORMATION COMPLEX;
D O I
10.1002/ajmg.1320440623
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Four unrelated cases of congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects were reported by McCredie and Reid in 1978 (J Pediatr 92: 762-765). As contiguous segments of the cervical neural crest are involved in the development of diaphragm and arms, the authors suggested that an early injury to the cervical neural crest might be the common underlying pathogenesis. We describe here a further example of this malformation complex: a newborn with a left posterolateral diaphragmatic hernia associated with ipsilateral thumb hypoplasia.
引用
收藏
页码:827 / 829
页数:3
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