- How does Gaucher disease affect the body?
- How is Gaucher disease prevented?
- Is Gaucher disease curable?
- How do you test for Gaucher disease?
- How would I know if I have an enlarged spleen?
- What is the life expectancy of someone with Gaucher disease?
- Does Gaucher disease cause weight gain?
- How common is Gaucher disease?
- Which ethnic group has the highest incidence of Gaucher disease?
- At what age is Gaucher disease diagnosed?
- What is the treatment for Gaucher disease?
- Is Gaucher disease an autoimmune disease?
- Who is affected by Gaucher disease?
- What are the signs and symptoms of Gaucher’s disease?
- How is Gaucher disease transmitted?
How does Gaucher disease affect the body?
Gaucher (go-SHAY) disease is the result of a buildup of certain fatty substances in certain organs, particularly your spleen and liver.
This causes these organs to enlarge and can affect their function.
The fatty substances also can build up in bone tissue, weakening the bone and increasing the risk of fractures..
How is Gaucher disease prevented?
There is no way to prevent Gaucher disease if you have the gene mutations. It’s wise to have testing if you are at risk. Early treatment may prevent damage to bones and organs from Gaucher disease type 1. If a DNA test shows that you’re a Gaucher carrier, and you’re planning on starting a family, talk to your provider.
Is Gaucher disease curable?
While there’s no cure for Gaucher disease, a variety of treatments can help control symptoms, prevent irreversible damage and improve quality of life.
How do you test for Gaucher disease?
An enzyme test called a beta-glucosidase leukocyte (BGL) test is the main tool that physicians use to diagnose Gaucher disease. This is because all patients with Gaucher disease will have low enzyme activity levels. Your physician can measure enzyme activity with a standard blood test.
How would I know if I have an enlarged spleen?
Symptoms you may experience with an enlarged spleen include: pressure or pain in the left upper part of your abdomen (near the stomach), feeling full without eating a large meal, or pain your left shoulder blade or shoulder area when taking a deep breath.
What is the life expectancy of someone with Gaucher disease?
Many people with Gaucher disease have few symptoms and can expect a normal lifespan even without treatment. One study estimated life expectancy at birth for people with type 1 Gaucher disease to be 68 years, compared with 77 years in the general population.
Does Gaucher disease cause weight gain?
People with GD may be at higher risk for certain medical issues, and a nutritious diet can keep them on a healthy path. Weight gain: People often gain weight after starting ERT, which can lead to an increase in fatty liver and a risk of developing fatty liver disease.
How common is Gaucher disease?
There are approximately 6,000 individuals with Gaucher disease in the United States. Gaucher disease is the most common genetic disorder of persons of Ashkenazic Jewish ancestry, where the incidence may be as high as 1 in 450 births.
Which ethnic group has the highest incidence of Gaucher disease?
Gaucher disease is considerably more common in the descendants of Jewish people from Eastern Europe (Ashkenazi), although individuals from any ethnic group may be affected. Among the Ashkenazi Jewish population, Gaucher disease is the most common genetic disorder, with an incidence of approximately 1 in 450 persons.
At what age is Gaucher disease diagnosed?
Although the disease can be diagnosed at any age, half of patients are under the age of 20 at diagnosis. The clinical presentation is heterogeneous with occasional asymptomatic forms.
What is the treatment for Gaucher disease?
Gaucher disease has no cure. Treatment options for types 1 and 3 include medicine and enzyme replacement therapy, which is usually very effective. There is no good treatment for the brain damage of types 2 and 3.
Is Gaucher disease an autoimmune disease?
A multicenter study shows that people with type 1 Gaucher disease (GD) may have higher levels of serum autoantibodies, but these patients showed no clinical signs of autoimmune disorders.
Who is affected by Gaucher disease?
Gaucher disease occurs in 1 in 50,000 to 100,000 people in the general population. Type 1 is the most common form of the disorder; it occurs more frequently in people of Ashkenazi (eastern and central European) Jewish heritage than in those with other backgrounds.
What are the signs and symptoms of Gaucher’s disease?
Symptoms of Gaucher disease can include:Enlarged spleen.Enlarged liver.Eye movement disorders.Yellow spots in the eyes.Not having enough healthy red blood cells (anemia)Extreme tiredness (fatigue)Bruising.Lung problems.More items…
How is Gaucher disease transmitted?
Gaucher disease is a genetic disorder transmitted in an autosomal recessive mode. An affected individual must inherit two recessive Gaucher genes—one from each parent—in order to have Gaucher disease. Individuals with only a single Gaucher gene are carriers.