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Yang, C. Acatalasemia. Encyclopedia. Available online: https://encyclopedia.pub/entry/4371 (accessed on 20 September 2026).
Yang C. Acatalasemia. Encyclopedia. Available at: https://encyclopedia.pub/entry/4371. Accessed September 20, 2026.
Yang, Catherine. "Acatalasemia" Encyclopedia, https://encyclopedia.pub/entry/4371 (accessed September 20, 2026).
Yang, C. (2020, December 23). Acatalasemia. In Encyclopedia. https://encyclopedia.pub/entry/4371
Yang, Catherine. "Acatalasemia." Encyclopedia. Web. 23 December, 2020.
Acatalasemia
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/acatalasemia

Acatalasemia is a condition characterized by very low levels of an enzyme called catalase. Many people with acatalasemia never have any health problems related to the condition and are diagnosed because they have affected family members.

genetic conditions

References

  1. Góth L, Eaton JW. Hereditary catalase deficiencies and increased risk ofdiabetes. Lancet. 2000 Nov 25;356(9244):1820-1.
  2. Góth L, Nagy T. Acatalasemia and diabetes mellitus. Arch Biochem Biophys. 2012Sep 15;525(2):195-200. doi: 10.1016/j.abb.2012.02.005.
  3. Góth L, Nagy T. Inherited catalase deficiency: is it benign or a factor invarious age related disorders? Mutat Res. 2013 Oct-Dec;753(2):147-54. doi:10.1016/j.mrrev.2013.08.002.
  4. Góth L, Rass P, Páy A. Catalase enzyme mutations and their association withdiseases. Mol Diagn. 2004;8(3):141-9. Review.
  5. Góth L. A new type of inherited catalase deficiencies: its characterizationand comparison to the Japanese and Swiss type of acatalasemia. Blood Cells MolDis. 2001 Mar-Apr;27(2):512-7.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Catherine Yang
View Times: 1.1K
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 04 Feb 2021
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