Literature DB >> 2400875

Hepatic imaging with computed tomography of chronic tyrosinaemia type 1.

D Macvicar1, C Dicks-Mireaux, J V Leonard, D G Wight.   

Abstract

Tyrosinaemia type 1 (fumaryl acetoacetase deficiency, hepato-renal tyrosinaemia) is a rare inborn error of metabolism which, in its chronic form, leads to cirrhosis in early childhood and subsequent development of hepatocellular carcinoma in a high proportion of cases. Imaging with computed tomography has an important role in assessing the progress of the liver disease and may be helpful in timing liver transplantation. The radiological features of seven cases are described and the implications discussed.

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Year:  1990        PMID: 2400875     DOI: 10.1259/0007-1285-63-752-605

Source DB:  PubMed          Journal:  Br J Radiol        ISSN: 0007-1285            Impact factor:   3.039


  3 in total

1.  Orthotopic liver transplantation in liver-based metabolic disorders.

Authors:  A P Mowat
Journal:  Eur J Pediatr       Date:  1992       Impact factor: 3.183

Review 2.  Organ transplantation for inherited metabolic disease.

Authors:  D A Kelly
Journal:  Arch Dis Child       Date:  1994-09       Impact factor: 3.791

3.  Self-induced correction of the genetic defect in tyrosinemia type I.

Authors:  E A Kvittingen; H Rootwelt; R Berger; P Brandtzaeg
Journal:  J Clin Invest       Date:  1994-10       Impact factor: 14.808

  3 in total

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