14q31
No treatment is available for Krabbe's disease.
i don't know how many children krabbe disease has
Children born with Krabbe's disease die in infancy.
Krabbe's disease is caused by a deficiency of the enzyme galactoside beta-galactosidase.
2-21
Tay-Sachs disease is caused by a genetic mutation in the HEXA gene on (human) chromosome 15 and no other chromosome is involved.
Tay-Sachs disease is caused by mutations in the HEXA gene located on chromosome 15. These mutations result in the absence or deficiency of the enzyme hexosaminidase A, leading to the accumulation of harmful substances in the brain and nervous system.
Kelly's son, Hunter, had Krabbe Disease and passed away at the age of 8 in 2005. Krabbe Disease is a degenerative disease of the central nervous system that destroys cells in the brain. There is no cure and, if present at birth, usually causes death by the age of 2.
Chromosome 4
Prognosis for infantile and juvenile Krabbe disease is very poor. Individuals with infantile type usually die at an average age of 13 months. Death usually occurs within a year after the child shows symptoms
Gaucher's disease is located on chromosome 1, which is not the sex chromosome, so no. It is not a sex linked disease.
Krabbe disease affects most ethnic groups equally (1 in every 100,000-200,000 births). However, there is an inbred community in Israel with a very high prevalence of the disease (6 in every 1,000 births) and some Scandinavian countries report an incidence of (1, in every 50,000 births).