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Defective in pompe's disease and tay-sachs disease?

Lysosomes are the organelles that become defective in these diseases.


Can a mother with a rare gentic disease pass it to her son?

A female who carries a defective recessive gene on one of her two X chromosomes has a 50% chance of passing the defective gene to her sons who will develop Fabry's disease associated with the defective gene.


What part of the cell is defective in pompe's disease and Tay Sachs disease?

Lysosomes


What do you call people that carry a defective gene but don't have the disease?

carrier


Having defective proteins in the cell membrane can cause disease?

True


Sickle-cell anemia is a disease passed by autosomal recessive inheritance. What is the likelihood that a person who has two parents with the disease will be a carrier of the defective gene?

If both parents have sickle-cell anemia, their child will inherit one copy of the defective gene from each parent, making them a carrier. Thus, the likelihood that a person who has two parents with the disease will be a carrier of the defective gene is 100%.


Is sickle cell anemia an deficiency disease?

The sickle cell anaemia is not a deficiency disease. It is a hereditary disease caused by defective gene in both the parents.


What disease is associated with blood sugar?

Diabetes is the primary disease associated with blood sugar.


What is a likelihood that a person who has two parents with the disease will be a carrier of the defective gene?

100%


What organelle is DNA Associated with?

nucleus


Is a deficiency disease in children characterized by defective bone growth?

Yes, rickets is a deficiency disease in children characterized by defective bone growth. It is primarily caused by a lack of vitamin D, calcium, or phosphorus, which are essential for bone development. Symptoms include bowed legs, delayed growth, muscle weakness, and dental problems.


What causes Fabry's disease?

Fabry's disease has an X-linked, recessive pattern of inheritance, meaning that the defective gene is carried on the X chromosome.