Datasets

3 datasets

HealthData.Gov

Enzyme replacement reverses abnormal cerebrovascular responses in Fabry disease

Background Fabry disease is a lysosomal X-linked enzyme deficiency of α-galactosidase A associated with an increased mortality and morbidity due to renal failure, cardiac disease and early onset stroke. Methods We…

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Updated Oct 29, 2026

HealthData.Gov

Arterial Wall Properties and Womersley Flow in Fabry Disease

Background Fabry disease is an X-linked recessive lysosomal storage disease resulting in the cellular accumulation of globotriaosylceramide particularly globotriaosylceramide. The disease is characterized by a dilated…

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Updated Oct 29, 2026

HealthData.Gov

Patients affected with Fabry disease have an increased incidence of progressive hearing loss and sudden deafness: an investigation of twenty-two hemizygous male patients

Background Fabry disease (FD, OMIM 301500) is an X-linked inborn error of glycosphingolipid metabolism due to the deficient activity of alpha-galactosidase A, a lysosomal enzyme. While the progressive systemic…

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Updated Oct 29, 2026