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What part of the cell is defective in pompe's disease and Tay-Sachs disease?
In Pompe's disease, the defect lies in the lysosomal enzyme alpha-glucosidase, which leads to the accumulation of glycogen in lysosomes. In Tay-Sachs disease, the defect is in the enzyme hexosaminidase A, which leads to the accumulation of GM2 gangliosides in lysosomes.
What is treatment for moyamoya disease?
There is no cure for moyamoya disease. Early treatment is important to avoid mental and physical impairment. Treatment options include medications and surgical revascularization
What is the treatment of disease with chemical substances called?
It is called chemical treatment
How long Colloidal Silver for Lyme Disease?
There is no scientific evidence to support the use of colloidal silver for Lyme disease treatment. It is important to consult with a healthcare professional for an appropriate and evidence-based treatment plan for Lyme disease.
Which pathogen has no treatment?
Prion diseases, such as Creutzfeldt-Jakob disease, currently have no known treatment that can effectively cure or stop the progression of the disease. Management focuses on symptom relief and supportive care for affected individuals.
How can one get Pompe disease?
Pompe disease is caused by a build up of glycogen (a type of sugar) in the cells, which causes muscles and organs not to function properly. Pompe disease is an inherited disease which means you can only get it from your parents when they both have a copy of the Pompe disease gene.
When was pompe disease discovered?
in 1932 by a dutch pathologist J Pompe
What organelle does pompe disease affect in cell?
lysosomes
Is pompe's disease related to lipids or carbohydrates?
yes
What part of the cell is defective in pompe's disease and Tay Sachs disease?
Lysosomes
Is pompe disease sex-linked?
No, Pompe disease is an autosomal recessive disorder, which means that both copies of the gene must be altered for a person to show symptoms. It is not linked to the sex chromosomes.
Defective in pompe's disease and tay-sachs disease?
Lysosomes are the organelles that become defective in these diseases.
Why did mrs Crowley decide to have another child if Megan had pompe disease?
Mrs. Crowley may have decided to have another child because she desired to expand her family or simply wanted another child despite the risk of the genetic disease. Additionally, Mrs. Crowley may have believed that advancements in medical research and treatment options for Pompe disease could provide better outcomes for a new child with the condition.
How do you find out you have Pompe Disease?
It took 3 muscle biopsies to diagnose my Pompe. Although I believe a blood spot test is the best way to diagnose it.
What organelle''pompe disease does affect in the cell and how does this disease affect someones life?
it is were it affects your repository system
What organelle does Pompe Disease affect in the cell and how does this disease affect someones life.?
it is were it affects your repository system
What organelle does Pompe Disease affect in the cell and how does this disease affect someones life?
it is were it affects your repository system
