Genetic counseling is advised for individuals with Gaucher disease and for their relatives to accurately assess risk and discuss testing options. For couples who previously had a child with Gaucher or in situations where both parents are.
Gaucher's Disease is Familial Splenic Anemia.
Gaucher Disease Treatment Program. http://gaucher.mgh.harvard.edu.
Symptoms of Gaucher disease can start in infancy, childhood, or adulthood.
Gaucher's disease is located on chromosome 1, which is not the sex chromosome, so no. It is not a sex linked disease.
The symptoms of Gaucher disease can be stopped and even reversed by treatment with injections of enzyme replacements.
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.
Three types of Gaucher disease have been identified, but there are many variations in how symptoms develop.
Gaucher disease
Lysosome
This disease affects males and females. 1 of 100 people in the United States are carries of the most common type of Gaucher disease
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
Gaucher disease is caused by a genetic defect in an enzyme called glucocerebroside. There are four different types of this disease. For more information about Gaucher disease visit Answers.com