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Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis

โœ Scribed by Verloes, A. ;Lambotte, C. ;Neri, Giovanni ;Reynolds, James F.

Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
918 KB
Volume
32
Category
Article
ISSN
0148-7299

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Congenital hepatic fibrosis (CHF) is probably the most common cause of non-icteric hepatosplenomegaly and is encountered mainly in children and young adults. We describe here two brothers from healthy, non-consanguineous parents. The patients showed early hepatosplenomegaly, portal hypertension, and