Familial Parkinson disease (Q41060): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Subtipo familiar da doença de Parkinson, um transtorno causado pela degeneração neuronal dopaminérgica progressiva da substância negra, que se caracteriza por tremor de repouso, bradicinesia e rigidez. Os casos familiares podem ser causados por mutações nos genes LRRK2, PARK7, PINK1, PRKN ou SNCA. | |||
| description / en | description / en | ||
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes. | |||
Revision as of 07:06, 13 August 2026
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A00.01 |
||
| English | Familial Parkinson disease |
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes. |
