Familial isolated pulmonary hypoplasia: a case report, suggesting autosomal recessive inheritance

Eur J Pediatr. 1994 Jun;153(6):460-3. doi: 10.1007/BF01983413.

Abstract

The exceptional observation of a healthy couple with two girls and a boy suffering from pulmonary hypoplasia and two normal children is reported. The affected infants died 1, 2 and 20 h after birth respectively. No other malformations were found. Histological findings suggest that the underdevelopment of the lungs has its origin at a more proximal level than the terminal bronchioles. Autosomal recessive inheritance is suggested.

Publication types

  • Case Reports

MeSH terms

  • Congenital Abnormalities / genetics
  • Fatal Outcome
  • Female
  • Humans
  • Infant, Newborn
  • Lung / abnormalities*
  • Male
  • Organ Size
  • Pulmonary Alveoli / pathology