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Original Article

Triosephosphate Isomerase Deficiency in a Child with Congenital Hemolytic Anemia and Severe Hypotonia

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Pages 553-556 | Received 11 Sep 1997, Accepted 17 Mar 1998, Published online: 09 Jul 2009

References

  • Schneider A S, Valentine W N, Hattori M, Hines HL, Jr. Hereditary hemolytic anemia with triose-phosphate isomerase deficiency. N Engl J Med. 1965; 272: 229–235
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  • Schneider A S, Dunn I, Ibsen K H, Weinstein I M. The pattern of glycolysis in erythrocyte triosephosphate isomerase deficiency. Clin Res. 1965; 13: 282
  • Valentine W M, Tanaka K R, Paglia D E. Pyruvate kinase and other enzyme deficiency disorders of the erythrocyte. The Metabolic Basis of Inherited Disease, 6th ed, CR Scriver, AL Beaudet, WS Sly, D Valle. McGraw-Hill, New York 1989; 2350–2351
  • Poll-The B T, Aicardi J, Girot R, Rosa R. Neurological findings in triosephosphate isomerase deficiency. Ann Neurol. 1985; 17: 439–443
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  • Clark A C, Szobolotzky M A. Triosephosphate isomerase deficiency: prenatal diagnosis. J Pediatr. 1985; 106: 417–421
  • Bellingham A J, Lestas A N, Williams L H, Nicolaides K. H. Prenatal diagnosis of a red-cell enzymopathy: triosephosphate isomerase deficiency. Lancet. 1989; 2: 419–421
  • Arya R, Lalloz M R, Nicolaides K H, Bellingham A J, Layton D M. Prenatal diagnosis of triosephosphate isomerase deficiency. Blood. 1996; 87: 4507–4509

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