Müller W D, Wendler H, Becker H
Klin Padiatr. 1978 Mar;190(2):129-32.
A case of congenital aplasia of the diaphragm with hypoplasia of both lungs is reported. By the complete absence of the diaphragm the liver could in the early stage of embryonic development expand around the heart into the thoracic cavity. This resulted in a growth arrest with consequently severe hypoplasia of both lungs, which were originally normally developed.
报告一例先天性膈肌发育不全合并双侧肺发育不全的病例。由于膈肌完全缺如,肝脏在胚胎发育早期可围绕心脏扩展至胸腔。这导致生长停滞,进而引起原本正常发育的双侧肺严重发育不全。