Resolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatoma

作者: David H. Van Thiel , Lawrence M. Gartner , Frank K. Thorp , Stephen L. Newman , Julie A. Lindahl

DOI: 10.1016/S0168-8278(86)80144-1

关键词:

摘要: The clinical history before transplantation and subsequent biochemical course of 3 children one adult with hereditary tyrosinemia treated by orthotopic hepatic is described. All four patients are now free their previous dietary restrictions appear to be cured both metabolic disease neoplasm.

参考文章(12)
L. Prive, Pathological findings in patients with tyrosinemia Canadian Medical Association Journal. ,vol. 97, pp. 1054- 1056 ,(1967)
A. Mortezai, M. Belanger, J. Larochelle, M. Tremblay, J. C. Claveau, G. Aubin, Experience with 37 infants with tyrosinemia. Canadian Medical Association Journal. ,vol. 97, pp. 1051- 1054 ,(1967)
André Grenier, André Lescault, Claude Laberge, Richard Gagné, Orvall Marner, Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemia Clinica Chimica Acta. ,vol. 123, pp. 93- 99 ,(1982) , 10.1016/0009-8981(82)90117-6
GÖRAN BODEGÅRD, JOHAN GENTZ, BENGT LINDBLAD, SVEN LINDSTEDT, ROLF ZETTERSTRÖM, Hereditary tyrosinemia. 3. On the differential diagnosis and the lack of effect of early dietary treatment. Acta Paediatrica. ,vol. 58, pp. 37- 48 ,(1969) , 10.1111/J.1651-2227.1969.TB04327.X
SVEN-PETTER FÄLLSTROM, BENGT LINDBLAD, GöRAN STEEN, ON THE RENAL TUBULAR DAMAGE IN HEREDITARY TYROSINEMIA AND ON THE FORMATION OF SUCCINYLACETOACETATE AND SUCCINYLACETONE1 Acta Paediatrica. ,vol. 70, pp. 315- 320 ,(1981) , 10.1111/J.1651-2227.1981.TB16558.X
E. Christensen, B.Brock Jacobsen, N. Gregersen, H. Hjeds, J.B. Pedersen, N.J. Brandt, Ulla B. Baekmark, Urinary excretion of succinylacetone and δ-aminolevulinic acid in patients with hereditary tyrosinemia Clinica Chimica Acta. ,vol. 116, pp. 331- 341 ,(1981) , 10.1016/0009-8981(81)90052-8
Arthur G. Weinberg, Charles E. Mize, Howard G. Worthen, The occurrence of hepatoma in the chronic form of hereditary tyrosinemia. The Journal of Pediatrics. ,vol. 88, pp. 434- 438 ,(1976) , 10.1016/S0022-3476(76)80259-4
R. Berger, O.P.A. Smit, S.A.Stoker-de Vries, M. Duran, D. Ketting, S.K. Wadman, DEFICIENCY OF FUMARYLACETOACETASE IN A PATIENT WITH HEREDITARY TYROSINEMIA Clinica Chimica Acta. ,vol. 114, pp. 37- 44 ,(1981) , 10.1016/0009-8981(81)90225-4
Gerald E Gaull, David K Rassin, Gail E Solomon, Ruth C Harris, John A Sturman, Biochemical Observations on So-called Hereditary Tyrosinemia Pediatric Research. ,vol. 4, pp. 337- 344 ,(1970) , 10.1203/00006450-197007000-00004