Leukodystrophy News and Research

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Leukodystrophies are inherited disorders that are characterized by a progressive breakdown (demyelination or hypomyelination) of the white matter in the central nervous system, caused by different mechanisms involving myelin proteins, as well as lipid and organic acid metabolism. They have to be distinguished from the “umbrella” term leukoencephalopathy, which is used to delineate any disease of the white matter.
Study identifies genetic mutation in the SPTSSA gene as cause of Hereditary Spastic Paraplegia

Study identifies genetic mutation in the SPTSSA gene as cause of Hereditary Spastic Paraplegia

Umbilical cord blood treats children born with non-cancerous genetic disorders

Umbilical cord blood treats children born with non-cancerous genetic disorders

TMEM106B gene reveals the causes of neurodegenerative diseases

TMEM106B gene reveals the causes of neurodegenerative diseases

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