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Clinical manifestations and natural history of Japanese heterozygous females with Fabry disease.

Source :
Current Medical Literature: Lysosomal Storage Disease. 2008, Vol. 8 Issue 1, p16-17. 2p.
Publication Year :
2008

Abstract

The article reports on the clinical features and natural history of Japanese heterozygous females with Anderson-Fabry disease (AFD). It states that acroparaesthesia and corneal opacities were the most common clinical manifestations, followed by proteinuria and left ventricular hypertrophy. It adds that as the clinical manifestations were found to develop increasingly with age, they underscore the need for monitoring as well as the introduction of enzyme therapy.

Details

Language :
English
ISSN :
14730901
Volume :
8
Issue :
1
Database :
Academic Search Index
Journal :
Current Medical Literature: Lysosomal Storage Disease
Publication Type :
Academic Journal
Accession number :
34849721