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Acatalasia
(Acatalasemia)
Summary
69
relevant articles (0 outcomes,
5 trials/studies)
found for this Disease
Description:
A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present.
Also Known As:
Acatalasemia; Hypocatalasemia; Hypocatalasia; Takahara Disease; Takahara's Disease Show All >>
Key Drugs and Agents for Acatalasia
Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
-
Catalase
:
4 studies in 55 results
: IBA
-
Hydrogen Peroxide (Hydroperoxide)
:
1 study in 5 results
: IBA
-
Messenger RNA (mRNA)
:
1 study in 2 results
: IBA
-
polyacrylamide
:
1 study in 1 result
: IBA
-
Mercury
:
5 results
: IBA
-
Glucosephosphate Dehydrogenase (Glucose 6 Phosphate Dehydrogenase)
:
3 results
: IBA
-
Amitrole (Aminotriazole)
:
3 results
: IBA
-
Complementary DNA (cDNA)
:
2 results
: IBA
-
DNA (Deoxyribonucleic Acid)
:
2 results
: IBA
-
Superoxide Dismutase
:
1 result
: IBA
Show All >>
Diseases Related to Acatalasia
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Acatalasia (Acatalasemia)
-
Zellweger Syndrome (Zellweger's Syndrome)
-
Fibrosis (Cirrhosis)
-
Inborn Genetic Diseases (Disease, Hereditary)
-
Rhizomelic Chondrodysplasia Punctata
Show All >>
Key Therapies for Acatalasia
Efficacy Chart >>
-
Peritoneal Dialysis
:
1 result
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