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Frontotemporal dementia ( FTD ), also called frontotemporal degeneration disease[ 1] or frontotemporal neurocognitive disorder,[ 2] encompasses several types of dementia involving the progressive degeneration of the brain's frontal and temporal lobes. [ 3] FTD is the second most prevalent type of early onset dementia after Alzheimer's disease ...
Niemann–Pick type C ( NPC) (colloquially, "Childhood Alzheimer's " [ 1]) is a lysosomal storage disease associated with mutations in NPC1 and NPC2 genes. Niemann–Pick type C affects an estimated 1:150,000 people. [ 2] Approximately 50% of cases present before 10 years of age, but manifestations may first be recognized as late as the sixth ...
Niemann–Pick disease (NP), also known as acid sphingomyelinase deficiency, is a group of rare genetic diseases of varying severity. These are inherited metabolic disorders in which sphingomyelin accumulates in lysosomes in cells of many organs.
Pick's disease, sporadic progressive supranuclear palsy, corticobasal degeneration, Parkinson-plus syndromes, dementia with Lewy bodies, Parkinson's disease, and multiple system atrophy. Treatment: Palliative and symptomatic interventions. Frequency: Estimated to affect 1 in 1 million people in the Netherlands.
Corticobasal degeneration. Corticobasal degeneration ( CBD) is a rare neurodegenerative disease involving the cerebral cortex and the basal ganglia. [ 1] CBD symptoms typically begin in people from 50 to 70 years of age, and typical survival before death is eight years.
Less common symptoms include extreme light sensitivity, dizziness and eye pain. The virus lives in animals like monkeys, birds, rodents and sloths, and is commonly spread to humans by infected ...
After the flu-like symptoms show up, people with mpox usually get a rash on the hands, feet, chest, face, or mouth or near the genitals, per the CDC. The rash can look like pimples or blisters ...
Sphingolipidoses are a class of lipid storage disorders or degenerative storage disorders caused by deficiency of an enzyme that is required for the catabolism of lipids that contain ceramide, [ 1] also relating to sphingolipid metabolism. The main members of this group are Niemann–Pick disease, Fabry disease, Krabbe disease, Gaucher disease ...