Find information on thousands of medical conditions and prescription drugs.

Fabry's disease

Fabry's disease (or Angiokeratoma corporis diffusum) is a lysosomal storage disease caused by deficient alpha galactosidase. more...

Home
Diseases
A
B
C
D
E
F
Fabry's disease
Facioscapulohumeral...
Factor V Leiden mutation
Factor VIII deficiency
Fallot tetralogy
Familial adenomatous...
Familial Mediterranean fever
Familial periodic paralysis
Familial polyposis
Fanconi syndrome
Fanconi's anemia
Farber's disease
Fascioliasis
Fatal familial insomnia
Fatty liver
Febrile seizure
Fibrodysplasia ossificans...
Fibromatosis
Fibrosarcoma
Fibrosis
Fibrous dysplasia
Filariasis
Fissured tongue
Fitz-Hugh-Curtis syndrome
Flesh eating bacteria
Fluorosis
Focal dystonia
Foix-Alajouanine syndrome
Follicular lymphoma
Fountain syndrome
Fragile X syndrome
Fraser syndrome
FRAXA syndrome
Friedreich's ataxia
Frontotemporal dementia
Fructose intolerance
Fructose-1,6-bisphosphatase...
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Medicines

Symptoms

Some of the pathological symtoms includes skin lesions, febrile episodes, burning in extremities. Skin lesions are painless elevated papules that appear all over body. Ocular involvement may present and showing vortex keratopathy. Death in early adulthood usually due to renal failure because of proteinuria induced hypertension.

Treatment

Treatment of Fabry's disease until recently was just symptomatic. This is changing with the drug Agalsidase beta (Fabrazyme®). Problematic is that the cost of the drug (approximately $170,000 US a year/patient) remains a barrier to many patients in some countries.

Read more at Wikipedia.org


[List your site here Free!]


Firms vie to treat genetic disease - Fabry's disease - Brief Article
From Science News, 11/4/00 by

Genzyme stands at the center of another enzyme-replacement story. The rare, fatal genetic condition in this instance is Fabry's disease. In people with the illness, lack of the enzyme alpha-galactosidase A results in an abnormal buildup of certain lipids in blood vessel cells. This causes episodes of severe pain and progressively damages the kidneys and heart.

Genzyme scientists and collaborators from Mt. Sinai Medical Center in New York City infused the missing enzyme into 29 adults with Fabry's disease. The treatment completely cleared the dangerous lipid in the hearts, kidneys, and skin of 20 patients. In all but one of the others, the treatment significantly slashed the lipid accumulation. Seeking approval for this therapy, Genzyme has submitted its data to the Food and Drug Administration.

Investigators from Transkaryotic Therapies (TKT) of Cambridge, Mass., and the National Institutes of Health have had similar success at treating Fabry's disease with alpha-galactosidase A. Like Genzyme, TKT has asked the FDA for an exclusive license for the therapy.

Adding to the corporate intrigue, Genzyme is suing TKT, claiming the company has infringed on its patents covering production of alpha-galactosidase A. TKT hasn't disclosed how it makes the enzyme, but the firm may be using its controversial technology known as gene activation. Most biotech firms produce a human protein by adding the gene that encodes it to animals or to cells growing in the laboratory. In contrast, TKT has developed methods to activate particular genes within human cells. With this strategy, TKT has sought to evade other companies' patents on several blockbuster drugs.

COPYRIGHT 2000 Science Service, Inc.
COPYRIGHT 2000 Gale Group

Return to Fabry's disease
Home Contact Resources Exchange Links ebay