Einstin
When did he discovered? Do you mean what? He discovered Yellow Fever was transmitted by mosquitoes. And if you mean when did he discover it, then the answer you are looking for is he led a research team that discovered this in 1900.
J.J.Thomson has discovered the electron in 1897
It is not known where exactly in England sodium was discovered. It was discovered by Sir Humphrey Davy in 1807.
Alexander Fleming discovered penicillin in 1928
cytoplasm/protoplasm was discovered by Robert brown
Canavan disease in Ashkenazi Jews, or globoid cell leukodystrophy (GLD) and metachromatic leukodystrophy (MLD) in Scandinavians.
The juvenile form of metachromatic leukodystrophy is characterized by gait disturbances, urinary incontinence, mental deterioration, and emotional difficulties
It was incorporated in 1982
I am not sure... Although, I suffer majorly from Hemi-Hyper Trophy. I am 13. It is very hard to deal with. Do you have Leukodystrophy oh Hemi-Hyper Trophy?
All types of leukodystrophy are genetic (present at conception), progressive, and never spontaneously resolve. None of the leukodystrophies can be cured, and effective treatments are limited.
Metachromatic leukodystrophy (MLD) is a rare degenerative neurological disease affecting the fatty covering that acts as an insulator around nerve fibers known as the myelin sheath.
Liver and kidney falure.
Adult metachromatic leukodystrophy is characterized by emotional disturbances and psychiatric symptoms. Disorders of movement and posture appear later. Dementia and decreased visual function also occur.
Metachromatic leukodystrophy (MLD), also called sulfatide lipidosis and arylsulfatase A (ARSA) deficiency, is inherited as an autosomal recessive trait, due to mutations in the arylsulfatase A (ARSA) gene
1. extensive idiopathic loss of myelin sheaths in the brain, as occurs in leukodystrophy.
1. extensive idiopathic loss of myelin sheaths in the brain, as occurs in leukodystrophy.
Leukodystrophy is a group of genetic disorders that affect the white matter of the brain, and its inheritance patterns can vary depending on the specific type. Some forms of leukodystrophy, particularly those that are X-linked or autosomal recessive, may appear to skip generations due to carrier status in unaffected family members. However, in cases of autosomal dominant leukodystrophies, the disorder typically does not skip generations, as affected individuals usually pass the trait to their offspring. Overall, the inheritance pattern can be complex, and genetic counseling is often recommended for families affected by these disorders.