Literature DB >> 8088304

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

B Frey1, A Fleischhauer, M Gersbach.   

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.

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Year:  1994        PMID: 8088304     DOI: 10.1007/bf01983413

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  5 in total

1.  Primary (isolated) bilateral pulmonary hypoplasia: a comparative study of radiologic findings and autopsy results.

Authors:  R Langer; H J Kaufmann
Journal:  Pediatr Radiol       Date:  1986

2.  Familial pulmonary hypoplasia.

Authors:  P Boylan; A Howe; J Gearty; N G O'Brien
Journal:  Ir J Med Sci       Date:  1977-06       Impact factor: 1.568

3.  Primary pulmonary hypoplasia in the neonate.

Authors:  L E Swischuk; C J Richardson; M M Nichols; M J Ingman
Journal:  J Pediatr       Date:  1979-10       Impact factor: 4.406

4.  Pulmonary hypoplasia resulting from phrenic nerve agenesis and diaphragmatic amyoplasia.

Authors:  J D Goldstein; L M Reid
Journal:  J Pediatr       Date:  1980-08       Impact factor: 4.406

5.  Primary pulmonary hypoplasia: report of a case with polyhydramnios.

Authors:  G Mendelsohn; G M Hutchins
Journal:  Am J Dis Child       Date:  1977-11
  5 in total
  3 in total

1.  Imaging of primary unilateral pulmonary hypoplasia: a case report.

Authors:  P Demaret; R Menten; C Debauche; S Moniotte
Journal:  Eur J Pediatr       Date:  2008-12-09       Impact factor: 3.183

2.  Severe primary pulmonary hypoplasia ("acinar dysplasia") in sibs: a genetically determined mesodermal defect?

Authors:  P Moerman; C Vanhole; H Devlieger; J P Fryns
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

3.  Familial primary pulmonary hypoplasia.

Authors:  B C Hamel
Journal:  Eur J Pediatr       Date:  1995-04       Impact factor: 3.183

  3 in total

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