de Groot R, Essed C E, Gaillard J L, Mettau J W, Villeneuve V H
Eur J Pediatr. 1984 Feb;141(4):248-9. doi: 10.1007/BF00572771.
A newborn infant with primary restrictive foramen ovale, tubular hypoplasia of the aortic arch, and some other developmental defects is described. This combination resulted in fetal hydrops, as was shown by ultrasonography. The child died 24 h after birth due to low output syndrome and extensive bronchopneumonia. The pathogenesis of this clinical entity is discussed.
描述了一名患有原发性卵圆孔狭窄、主动脉弓管状发育不全及其他一些发育缺陷的新生儿。超声检查显示，这种情况导致了胎儿水肿。该患儿出生后24小时因低输出量综合征和广泛支气管肺炎死亡。本文讨论了这一临床实体的发病机制。
