Literature DB >> 10460304

[Acatalasemia--Takahara's disease].

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.

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Year:  1999        PMID: 10460304     DOI: 10.1007/s001050050964

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  2 in total

1.  In reply.

Authors:  Christos C Zouboulis
Journal:  Dtsch Arztebl Int       Date:  2015-03-27       Impact factor: 5.594

Review 2.  Catalase enzyme mutations and their association with diseases.

Authors:  László Góth; Péter Rass; Anikó Páy
Journal:  Mol Diagn       Date:  2004
  2 in total

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