Hereditary tyrosinaemia. Clinical, enzymatic, and pathological study of an infant with the acute form of the disease.

Author:

Carson N A,Biggart J D,Bittles A H,Donovan D

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference31 articles.

1. A case of congenital cirrhosis of the liver with renal tubular defects akin to those in the Fanconi syndrome;Baber, M.D.;Archives of Disease in Childhood,1956

2. Infantile lactic acidosis due to hereditary fructose 1, 6-diphosphatase deficiency;Baerlocher, K.; Gitzelmann, R.; Nuissli, R.; Dumermuth, G.;Helvetica Paediatrica Acta,1971

3. Fructose-1, 6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of 'Tyrosinosis';Bakker, H.D.; DeBree, P.K.; Ketting, D.; Van Sprang, F.J.; Wadman, S.K.;Clinica Chimica Acta,1974

4. Hereditary tyrosinemia. III: On the differential diagnosis and the lack of effect of early dietary treatment;Bodegard, G.; Gentz, J.; Lindblad, B.; Lindstedt, S.; Zetterstrom, R.;Acta Paediatrica Scandinavica,1969

5. Discussion on Tyrosinosis. Biochemical and dietary studies;Carpenter, G.;Pediatric Research,1968

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