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Acatalasia

Known as: Acatalasemia, CATALASE DEFICIENCY, Takahara's Disease 
A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and… 
National Institutes of Health

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Acatalasemia Japanese typeHypocatalasemia
Catalase deficiencyIn BloodMicrobiologicalchemically induced

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Increased Susceptibility to Oxidant-Mediated Tissue Injury and Peritoneal Fibrosis in Acatalasemic Mice
Background: Peritoneal fibrosis is a major complication leading to the loss of peritoneal function in patients undergoing… 
2000
2000
Lipid and carbohydrate metabolism in acatalasemia.
Oxidative stress appears to be involved in degenerative diseases, including atherosclerosis and some forms of diabetes mellitus… 
1997
1997
Polymorphism of 5′ of the catalase gene in Hungarian acatalasemia and hypocatalasemia
The amplified fragment length polymorphism of Hinfl on the promoter region of the catalase gene in Hungarian acatalasemic and… 
1995
1995
A novel human catalase mutation (358 T-->del) causing Japanese-type acatalasemia.
Japanese-type acatalasemia is characterized by the almost total loss of catalase activity in red cells and is often associated… 
1992
1992
Two cases of acatalasemia in Hungary.
  • L. Góth
  • Clinica chimica acta; international journal of…
  • 1992
  • Corpus ID: 29438724
1987
1987
Isolation of a cDNA clone for murine catalase and analysis of an acatalasemic mutant.
1983
1983
Ether link cleavage is the major pathway of iodothyronine metabolism in the phagocytosing human leukocyte and also occurs in vivo in the rat.
These studies were performed to test the hypothesis that ether link cleavage (ELC) is an important pathway for the metabolism of… 
1979
1979
Acatalasia in two Peruvian siblings.
The oral findings in two Peruvian brothers, 10- and 11-years-old, with acatalasia are presented. Gingival necrosis and severe… 
1968
1968
Position of the acatalasemia gene in linkage group V of the mouse.
1961
1961
Two cases of acatalasia in Switzerland
Es wird über 2 Fälle von Akatalasie, einem seltenen, bisher ausschliesslich bei Japanern beobachteten Enzym-Defekt, berichtet4. 
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