Acatalasia is an autosomal recessive peroxisomal disorder caused by absent or very low levels of the enzyme catalase. Catalase breaks down hydrogen peroxide...
5 KB (412 words) - 01:13, 25 February 2024
Catalase (section Acatalasia)
liver, and type 2 diabetes. Some humans have very low levels of catalase (acatalasia), yet show few ill effects. The increased oxidative stress that occurs...
39 KB (4,262 words) - 01:45, 14 August 2024
Name OMIM Gene ICD-10 NA Pipecolic acidemia 600964 PHYH E80.301 Acatalasia 115500 CAT E80.310 Hyperoxaluria type 1 259900 AGXT E80.311 Acyl-CoA oxidase...
8 KB (578 words) - 19:15, 22 July 2024
involve the moist linings of the eyes, nose, mouth, genitals, and anus. Acatalasia (acatalasemia, Takahara's disease) Acquired dyskeratotic leukoplakia Actinic...
198 KB (17,958 words) - 01:24, 6 July 2024
in determining cardiac complications in COVID-19. Antioxidative stress Acatalasia Bruce Ames Malondialdehyde, an oxidative stress marker Mitochondrial free...
55 KB (6,161 words) - 22:43, 25 June 2024
environment on genes. In his early work, he studied sickle-cell disease and acatalasia. conducted research on the effects of radiation on survivors of the Hiroshima...
16 KB (1,912 words) - 05:12, 3 June 2024
the general public. Takahara Shigeo - One‐time Professor who discovered Acatalasia Official site Official site (in Japanese) Medical Museum 34°37′55″N 133°48′41″E...
4 KB (363 words) - 12:32, 24 April 2024
320.565.556.750 – peroxisomal disorders MeSH C16.320.565.556.750.025 – acatalasia MeSH C16.320.565.556.750.112 – adrenoleukodystrophy MeSH C16.320.565.556...
78 KB (6,496 words) - 05:23, 12 April 2022
452.648.556.750 – peroxisomal disorders MeSH C18.452.648.556.750.025 – acatalasia MeSH C18.452.648.556.750.112 – adrenoleukodystrophy MeSH C18.452.648.556...
47 KB (4,274 words) - 16:49, 9 February 2024