MYOCARDIAL DYSGENESIS WITH PERSISTENT SINUSOIDS IN A NEONATE WITH NOONANS PHENOTYPE

被引:27
作者
AMANN, G
SHERMAN, FS
机构
[1] CHILDRENS HOSP PITTSBURGH,DEPT PATHOL,PITTSBURGH,PA
[2] MAGEE WOMENS HOSP,DEPT PERINATAL CARDIOL,PITTSBURGH,PA 15213
[3] UNIV PITTSBURGH,SCH MED,PITTSBURGH,PA 15261
来源
PEDIATRIC PATHOLOGY | 1992年 / 12卷 / 01期
关键词
ABNORMAL MYOCARDIAL DEVELOPMENT; CONGENITAL HEART BLOCK; MYOCARDIAL DYSGENESIS; NOONAN SYNDROME; PERSISTENT MYOCARDIAL SINUSOIDS;
D O I
10.3109/15513819209023283
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Structural cardiac anomalies indicative of primary myocardial maldevelopment are reported in a newborn girl with congenital heart block. The cardiac findings included disordered trabeculation of both ventricles with persistent intramyocardial sinusoids, hypoplastic papillary muscles, and dysplastic atrioventricular valves with partial downward displacement of the septal leaflet of the tricuspid valve. Dilatation of the ascending aorta and craniofacial dysmorphism including webbed neck, hypertelorism, and low-set ears raise the possibility of Noonan syndrome.
引用
收藏
页码:83 / 92
页数:10
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