Fabry disease |
Alpha-galactosidase A deficiency; Anderson-Fabry Disease; Angiokeratoma Corporis Diffusum; Angiokeratoma diffuse; Ceramide trihexosidase deficiency; Fabry's Disease; Fabry//'s Disease; GLA deficiency; Hereditary dystopic lipidosis |
Fabry disease is an inherited disorder caused by the buildup of a particular type of fat (lipid) in the body's cells. This buildup results in pain, particularly in the hands and feet; clusters of small, dark red spots (angiokeratomas) on the skin; a decreased ability to sweat (hypohidrosis); cloudiness of the front part of the eye (the cornea); and hearing loss. Fabry disease also involves potentially life-threatening complications such as progressive kidney damage, heart attack, and stroke. Milder forms of the disorder may appear later in life and affect the heart or kidneys only.
Fabry's disease (also known as Anderson-Fabry disease, Angiokeratoma corpor ...
From the WEST scientific·clinical |
From the EAST traditional·alternative |
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Fabry disease Other1-2 of 4 more...
Treating Rare Lysosomal Storage Diseases
... When waste is created in the world, if it is not removed or destroyed, terrible things can happen: diseases fester, rodent populations soar, people sicken and die. Within the world of the body, when w...
Source: Cleveland Clinic
Fabry''s Disease ... What is Fabry''s Disease? Fabry disease is a fat storage disorder caused by a deficiency of an enzyme involved in the biodegradation of lipids. The gene that is altered in this disorder is on the X-ch...
Source: Cleveland Clinic
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Fabry disease Articles
- Fabry disease
... Fabry disease is an inherited disorder caused by the buildup of a particular type of fat (lipid) in the body's cells. This buildup results in pain, particularly in the hands and feet; clusters of ...

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