Fabry disease is a rare genetic disease that results from abnormal buildup of a type of fat called globotriaosylceramide (Gb3…
Articles by Vaidyanathan
Fabry disease is a rare genetic disease in which mutations in the GLA gene lead to the accumulation…
Fabry disease is a rare genetic disorder characterized by the accumulation of a type of fat called…
Fabry disease is a lysosomal storage disorder caused by mutations in the GLA gene. These mutations result in…
Fabry disease is a rare genetic disease that occurs as a result of a mutation in the GLA…
Enzyme replacement therapy (ERT), such as Fabrazyme, addresses the primary cause of Fabry disease — mutations in…
Heart disease is common in Fabry disease patients, and those with the disease should be vigilant about taking steps…
Kidney problems are common in people with Fabry disease. They are caused by the deposition of certain fatty molecules, known…
Fabry disease is a rare X-linked genetic disorder characterized by the inability of the body to break down…
Fabry disease is a rare X-linked genetic disease characterized by the buildup of a type of fat called…