Abstract
105 babies with neonatal hepatitis were studied carefully and followed for up to 11 1/2 years. Ascertainment was complete for those with severe and persistent jaundice, but less complete for mild or anicteric cases. Prognosis was found to be poor (40% death or cirrhosis) in babies with perisitently acholic stools, but relatively good (less than 15% death or cirrhosis) in those with jaundice which was less persistent and less obstructive. The presence of second diseases (including alpha1-antitrypsin deficiency or a family history of other affected children) seemed to play a part in determining poor prognosis. A distinctive group of babies (22 cases) presented with acute fulminant illness (with or without jaundice) in the neonatal period. Cytomegalovirus infection carried a relatively good prognosis. Guidelines for selection of patients for therapeutic trials are suggested.
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Selected References
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- Alagille D., Odièvre M., Gautier M., Dommergues J. P. Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. J Pediatr. 1975 Jan;86(1):63–71. doi: 10.1016/s0022-3476(75)80706-2. [DOI] [PubMed] [Google Scholar]
- Danks D. M., Campbell P. E., Jack I., Rogers J., Smith A. L. Studies of the aetiology of neonatal hepatitis and biliary atresia. Arch Dis Child. 1977 May;52(5):360–367. doi: 10.1136/adc.52.5.360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Danks D. M. Management of newborn babies in whom serious metabolic illness is anticipated. Arch Dis Child. 1974 Jul;49(7):576–578. doi: 10.1136/adc.49.7.576. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LONGMIRE W. P., Jr CONGENITAL BILIARY HYPOPLASIA. Ann Surg. 1964 Mar;159:335–343. doi: 10.1097/00000658-196403000-00002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oberklaid F., Danks D. M., Davies H. E. Problems encountered in the diagnosis of galactosaemia. Aust Paediatr J. 1976 Mar;12(1):14–18. [PubMed] [Google Scholar]
- Reed G. B., Butt E. M., Landing B. H. Copper in childhood liver disease. A histologic, histochemical, and chemical survey. Arch Pathol. 1972 Mar;93(3):249–255. [PubMed] [Google Scholar]
- Thaler M. M., Gellis S. S. Studies in neonatal hepatitis and biliary atresia. 3. Progression and regression of cirrhosis in biliary atresia. Am J Dis Child. 1968 Sep;116(3):271–279. doi: 10.1001/archpedi.1968.02100020273007. [DOI] [PubMed] [Google Scholar]
