Fabry disease

Overview

Are there other names for Fabry disease?

Fabry disease can also be referred to as:

  • Alpha-Galactosidase A deficiency
  • Anderson-Fabry disease
  • Angiokeratoma corporis diffusum
  • Angiokeratoma diffuse
  • Ceramide trihexosidase deficiency
  • Fabry's disease
  • GLA deficiency
  • Hereditary dystopic lipidosis
  • Fabry
  • Late onset Fabry disease
  • Later onset Fabry disease
  • Classic Fabry disease
  • Non-classic Fabry disease

SOURCE: Emory University - Department of Human Genetics in collaboration with ThinkGenetic • https://www.thinkgenetic.com/diseases/fabry-disease/overview/558 • DATE UPDATED: 2019-12-12

References

Fabry disease - Genetics Home Reference - NIH. (2019, November 12). Retrieved November 22, 2019, from http://ghr.nlm.nih.gov/condition/fabry-disease.

National Fabry Disease Foundation. Retrieved from http://www.fabrydisease.org.

Fabry disease revisited: Management and treatment recommendations for adult patients. Ortiz A, Germain DP, Desnick RJ, Politei J, Mauer M, Burlina A, Eng C, Hopkin RJ, Laney D, Linhart A, Waldek S, Wallace E, Weidemann F, Wilcox WR. Mol Genet Metab. 2018 Apr;123(4):416-427. doi: 10.1016/j.ymgme.2018.02.014. Epub 2018 Feb 28. Review. https://www.sciencedirect.com/science/article/pii/S1096719217307680?via%3Dihub Retrieved 12DEC19.

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