Condition

Transaldolase deficiency

Endocrine, Nutritional and Metabolic Diseases

Transaldolase deficiency is a disease characterised by abnormally low levels of the transaldolase enzyme, a metabolic enzyme involved in the pentose phosphate pathway. It is caused by a mutation in the transaldolase gene, called TALDO1. The condition was first described by Verhoeven and colleagues in 2001. Because the enzyme takes part in the pentose phosphate pathway, a core route of carbohydrate metabolism, the disorder is classed among the inherited metabolic diseases, and it is defined by the enzyme shortfall and the gene change that produces it rather than by one single clinical sign.

Facts
Classification
ICD-10 Chapter
IV: Endocrine, Nutritional and Metabolic Diseases 1
First Described
2001 2
Prevalence Band
Rare (Under 1 in 2000) 3
Causative Agent
Causative Agent (category)
Genetic / Hereditary 2
Sources
1. Orphadata (Orphanet): Orphadata cross-references for ORPHA:101028 Transaldolase deficiency
Orphadata (Orphanet)ICD-10 cross-reference
Quote, ICD-10 cross-reference
"Reference": "E74.8", "Source": "ICD-10"
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2. Transaldolase deficiency (Wikipedia)
  • Lead paragraph
    It is caused by mutation in the transaldolase gene (TALDO1).
  • Lead paragraph [first-described-year]
    It was first described by Verhoeven et al. in 2001.
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3. Orphadata (Orphanet): Orphadata epidemiology for ORPHA:101028 Transaldolase deficiency
Orphadata (Orphanet)Prevalence, Worldwide
Quote, Prevalence, Worldwide
"PrevalenceClass": "\u003c1 / 1 000 000", "PrevalenceGeographic": "Worldwide"
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