Literature DB >> 7114003

Triosephosphate isomerase deficiency. A case report with neuropathological findings.

S A Clay, N A Shore, B H Landing.   

Abstract

A 12-year-old girl had chronic nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency. Developmental and motor delay and muscular weakness were followed by cerebellar dysfunction and finally spasticity with hyperreflexia. Abnormal histopathological findings were hyaline cell bodies and axonal "spheroids" in the hypothalamus and cerebellar cortex, severe neuronal loss in the dentate and olivary nuclei, and partial loss of cerebellar Purkinje's and granular layer cells (olivocerebellar atrophy).

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Year:  1982        PMID: 7114003

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  9 in total

1.  Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany--a study of 3000 people.

Authors:  S W Eber; M Dünnwald; G Heinemann; T Hofstätter; H M Weinmann; B H Belohradsky
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  Hereditary triose phosphate isomerase deficiency: seven new homozygous cases.

Authors:  R Rosa; M O Prehu; M C Calvin; J Badoual; D Alix; R Girod
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.

Authors:  S W Eber; A Pekrun; A Bardosi; M Gahr; W K Krietsch; J Krüger; R Matthei; W Schröter
Journal:  Eur J Pediatr       Date:  1991-09       Impact factor: 3.183

4.  Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.

Authors:  A Bardosi; S W Eber; M Hendrys; A Pekrun
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

5.  Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus.

Authors:  S Merkle; W Pretsch
Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

6.  Premature translation termination mediates triosephosphate isomerase mRNA degradation.

Authors:  I O Daar; L E Maquat
Journal:  Mol Cell Biol       Date:  1988-02       Impact factor: 4.272

7.  Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms.

Authors:  S Hollán; H Fujii; A Hirono; K Hirono; H Karro; S Miwa; V Harsányi; E Gyódi; M Inselt-Kovács
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

8.  Human triosephosphate isomerase deficiency resulting from mutation of Phe-240.

Authors:  M L Chang; P J Artymiuk; X Wu; S Hollán; A Lammi; L E Maquat
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

9.  Bone marrow transplantation corrects haemolytic anaemia in a novel ENU mutagenesis mouse model of TPI deficiency.

Authors:  Ashlee J Conway; Fiona C Brown; Elinor J Hortle; Gaetan Burgio; Simon J Foote; Craig J Morton; Stephen M Jane; David J Curtis
Journal:  Dis Model Mech       Date:  2018-05-21       Impact factor: 5.758

  9 in total

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