| Literature DB >> 10460304 |
H Perner1, C Krenkel, B Lackner, H Hintner, T Hawranek.
Abstract
The case of a 30 year old man with acatalasemia is presented. The congenital disorder is charaterized by a lack or major reduction of catalase, an enzyme that catalyzes the decomposition of hydrogen peroxide to oxygen and water. The defect is inherited in an autosomal recessive fashion. Occasionally the defect manifests as progressive oral gangrene or Takahara's, disease.Entities:
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Year: 1999 PMID: 10460304 DOI: 10.1007/s001050050964
Source DB: PubMed Journal: Hautarzt ISSN: 0017-8470 Impact factor: 0.751