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The newest form of treatment for Gaucher disease is enzyme replacement therapy, in which GC can be administered intravenously. The enzyme can be prepared either by purification from placentas (alglucerase) or by.

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Does a treatment exist for gauches disease?

Treatment but not a cure - and it is spelled Gaucher's disease.


How is Gaucher disease treated?

The symptoms of Gaucher disease can be stopped and even reversed by treatment with injections of enzyme replacements.


What has the author Carol Kari written?

Carol Kari has written: 'Understanding Gaucher disease' -- subject(s): Gaucher's disease, Genetic aspects, Genetic aspects of Gaucher's disease, Inborn errors of Metabolism, Metabolism, Inborn errors of, Treatment


What is the prognosis for Type 1 Gaucher disease?

With treatment and control of symptoms, people with Type 1 Gaucher disease may lead fairly long and normal lives.


What is the contact information for the Gaucher Disease Treatment Program?

The contact information for the Gaucher Disease Treatment Program varies depending on the specific institution or facility offering the program. You can typically find contact information on the website of the hospital or medical center providing the program. It is recommended to reach out directly to the healthcare provider for the most accurate and up-to-date contact details.


Is gaucher's Disease caused by heredity?

Gaucher's Disease is Familial Splenic Anemia.


What is the treatment for Gaucher disease?

Symptomatic treatment may include blood transfusions to treat anemia, removal of the enlarged spleen, and joint replacement.


What has the author Jackie Bryant written?

Jackie Bryant has written: 'Ceredase in the treatment of Type 1 Gaucher's disease'


When do symptoms of Gaucher disease first appear?

Symptoms of Gaucher disease can start in infancy, childhood, or adulthood.


Is gaucher disease-sex linked?

Gaucher's disease is located on chromosome 1, which is not the sex chromosome, so no. It is not a sex linked disease.


Who discovered the Gaucher's disease?

Gaucher disease is the most common lysosomal storage disease. It was named for the French physician Phillipe Gaucher who first described it in 1882. The disease is caused by a lack of glucocerebrosidase, which causes a buildup of glucocerebroside in the tissues.


How many types of Gaucher disease are there?

Three types of Gaucher disease have been identified, but there are many variations in how symptoms develop.