VATER VACTERL ASSOCIATION - CLINICAL VARIABILITY AND EXPANDING PHENOTYPE INCLUDING LARYNGEAL STENOSIS

被引:27
作者
CORSELLO, G
MARESI, E
CORRAO, AM
DIMITA, U
LOCASCIO, M
CAMMARATA, M
GIUFFRE, L
机构
[1] OSPED BUCCHERI LA FERLA,DIV NEONATOL,PALERMO,ITALY
[2] UNIV PALERMO,IST ANAT PATOL,I-90142 PALERMO,ITALY
[3] OSPED BAMBINI G DI CRISTINA,DIV CHIRURG PEDIAT,PALERMO,ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 44卷 / 06期
关键词
BLASTOGENESIS; CONGENITAL ABNORMALITIES; TRACHEOESOPHAGEAL MALFORMATIONS;
D O I
10.1002/ajmg.1320440619
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Vertebral abnormalities and anorectal and tracheoesophageal defects are the main manifestations in the VATER/VACTERL association. Radial defects vary from radial aplasia to thumb duplication. Heart and renal defects are reported with lower frequency. Additional malformations, such as the laryngeal stenosis described in the present patient, may expand the phenotype of the association. The wide spectrum of congenital abnormalities confirms the high clinical variability of VATER/VACTERL association which seems to be due to a disruption of blastogenesis.
引用
收藏
页码:813 / 815
页数:3
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