| Literature DB >> 24558776 |
Vanja Basić Kes1, Marijan Cesarik2, Iris Zavoreo1, Silva Soldo-Butković3, Petar Kes4, Nikolina Basić-Jukić4, Sanjin Racki5, Marko Jakić6, Diana Delić-Brkljacić7, Zlatica Jukić8, Zlatko Trkanjec1, Vesna Serić1, Vesna Vargek Solter1, Ivan Bielen9, Silvio Basić10, Vida Demarin11.
Abstract
Fabry disease (Anderson-Fabry disease) is one of the most common lysosomal storage diseases (after Gaucher disease) caused by deficient activity of the alpha-galactosidase A (alpha-Gal A) enzyme, which leads to progressive accumulation of globotriaosylceramide in various cells, predominantly in endothelium and vascular smooth muscles, with multisystem clinical manifestations. Estimates of the incidence range from one per 40,000 to 60,000 in males, and 1:117,000 in the general population. Pain is usually the first symptom and is present in 60%-80% of affected children, as well as gastrointestinal disturbances, ophthalmologic abnormalities and hearing loss. Renal failure, hypertrophic cardiomyopathy, or stroke as the presenting symptom may also be found even as isolated symptoms of the disease. Life expectancy is reduced by approximately 20 years in males and 10-15 years in females, therefore enzyme replacement therapy should be introduced in patients of any age and either sex, who meet treatment criteria for Anderson-Fabry disease.Entities:
Mesh:
Year: 2013 PMID: 24558776
Source DB: PubMed Journal: Acta Clin Croat ISSN: 0353-9466 Impact factor: 0.780