Archives of Disease in Childhood · 1973 · 266 citations · 16 references
MedicineGeneticsPediatricsHepatologyHuman GeneticsPediatric GeneticsCongenital AnomaliesCongenital DisordersCongenital MalformationsPediatric Liver DiseaseVascular AnomaliesVascular MalformationsAutosomal Dominant InheritanceCongenital Cardiovascular MalformationsCongenital Liver MalformationsCongenital Vascular AnomaliesNeonatal HepatitisObstructive JaundicePulmonary Artery AnomaliesVariable Penetrance
A new syndrome is described of which the salient features are (1) congenital hypoplasia and stenoses of the pulmonary arteries, sometimes with associated cardiovascular malformations; (2) neonatal liver disease, commonly with obstructive jaundice and resembling biliary atresia or neonatal hepatitis, but sometimes apparent only as mild persistent hepatic dysfunction; and (3) various minor congenital anomalies, including an odd facies. There is a familial tendency suggesting autosomal dominant inheritance, with variable penetrance.
16
Atresia of the intrahepatic dile ducts.
E. H. Ahrens, Ruth C. Harris, Heber MacMahon · PubMed · 1951 · 84 citations
Daniel Stowens · Annals of the New York Academy of Sciences · 1963 · 71 citations
Persistent jaundice in infancy
Robert L. Brent, James B. Arey, William A. Blanc et al. · The Journal of Pediatrics · 1962 · 70 citations
Medicine, Child Health, Pediatrics +10