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what is 'Gaucher disease - inherited metabolic disorder with accumulation of fat in tissues '?

Definition for Gaucher disease

Gaucher's disease (pronounced goʃeɪ) is the most common of the lipid storage diseases. It is caused by a deficiency of the enzyme glucocerebrosidase, leading to an accumulation of its substrate, the fatty substance glucocerebroside. more

do i have 'Gaucher disease'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'Gaucher disease'
1 - 5 of 32 diagnostic tests
Blood B-Glucosidase
Molecular Genetic Studies
Abdominal CAT Scan
Abdominal ultrasonography
Ultrasound of abdominal contents
Chest X-ray
Radiological technique to image the chest
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therapeutic procedures for 'Gaucher disease'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Gaucher disease:


medications search results for 'Gaucher disease'
1 - 2 of 2 medications
rankings are computer generated. please consult your health care provider.
  imiglucerase (a.k.a imiglucerase, Cerezyme)
  miglustat (a.k.a miglustat, Zavesca)



web search results for 'Gaucher disease'?
Results 1 - 50 - Gaucher disease
ghr.nlm.nih.gov - summary
health.yahoo.com - summary
www.medicinenet.com - summary
www.ncbi.nlm.nih.gov - summary
www.nlm.nih.gov - summary
adam.about.com - summary


quick facts
category
genetic or congenital
metabolic
frequency
uncommon (U.S.)
likelihood by age
likelyhood by duration of symptoms
some common symptoms
short stature
stomach swelling
ulcer(s) on leg(s) and feet
vision problems
some related diagnoses
Down's Syndrome
DiGeorge's Syndrome
autosomal dominant polycystic kidney disease
APC resistance
more
related physician types
genetics specialist
family practitioner
internist
show local physicians
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The results are computer generated suggestions to help you find a physician. MEDgle does not recommend any particular type of physician or claim to be complete or accurate in the providers and specialties suggested.


GENETIC OR CONGENITAL METABOLIC
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