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Fabry disease
- Fabry disease is an inherited disorder that results from the buildup of a type of fat, called globotriaosylceramide, in the body's cells. Beginning in childhood, ...
- Lipid Storage Diseases (National Institute of Neurological Disorders and Stroke)National Institute of Neurological Disorders and Stroke ... Leukodystrophies/Specifics ... Leukodystrophies ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders
- ... GLA gene have been identified in people with Fabry disease. Most of these genetic changes are unique to ... leading to the varied signs and symptoms of Fabry disease.Mutations that eliminate the activity of the alpha- ...
- Pegunigalsidase alfa-iwxj injection is used to treat Fabry disease (an inherited condition in which a type of ...
- Agalsidase beta injection is used to treat Fabry disease (an inherited condition in which a type of fatty substance builds up in the body, resulting in nerve and organ damage) in adults ...
- Disease Treatments (American Society of Gene & Cell Therapy)American Society of Gene & Cell Therapy ... Genes and Gene Therapy/Specifics ... Genes and Gene Therapy
- ... Blood Clot Alliance National Down Syndrome Society National Fabry Disease Foundation National Fragile X Foundation National Gaucher Foundation ...
- ... of this condition include a metabolic disorder called Fabry disease, immune disorders such as celiac disease or Sjogren ...
- Genetic Brain Disorders (National Library of Medicine)A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
- National Kidney Foundation (National Kidney Foundation)... Pressure/Hypertension Diabetes Type 1 Diabetes Type 2 Fabry Disease FSGS (Focal Segmental Glomerulosclerosis) Glomerulonephritis Goodpasture's Syndrome HIV/ ...