Beckwith-Wiedemann Syndrome with Unusual Hepatic and Pancreatic Features: A Case Expanding the Phenotype
We describe an infant with Beckwith-Wiedemann syndrome (BWS) who had hepatic and pancreatic findings not previously described in BWS. These were biliary dysgenesis and enlargement and cystic dysplasia of the pancreas. The biliary dysgenesis was characterized by proliferation of abnormally shaped duc...
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Veröffentlicht in: | Fetal and pediatric pathology 1990, Vol.10 (4), p.593-600 |
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Sprache: | eng |
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