Parkinsonian Disorders [parkinsonské poruchy]

topical
301
Terms

autosomálně dominantní juvenilní parkinsonismus
autosomálně dominantní juvenilní Parkinsonova choroba
autosomálně dominantní juvenilní Parkinsonova nemoc
autosomálně dominantní parkinsonismus
autosomálně recesivní juvenilní parkinsonismus
autosomálně recesivní juvenilní Parkinsonova choroba
autosomálně recesivní juvenilní Parkinsonova nemoc
autosomálně recesivní parkinsonismus
autozomálně dominantní juvenilní parkinsonismus
autozomálně dominantní juvenilní Parkinsonova choroba
autozomálně dominantní juvenilní Parkinsonova nemoc
autozomálně dominantní parkinsonismus
autozomálně recesivní juvenilní parkinsonismus
autozomálně recesivní juvenilní Parkinsonova choroba
autozomálně recesivní juvenilní Parkinsonova nemoc
autozomálně recesivní parkinsonismus
experimentální parkinsonismus vyvolaný methylphenyltetrahydropyridinem
experimentální parkinsonismus vyvolaný MPTP
familiární juvenilní parkinsonismus
parkinsonismus experimentální
parkinsonismus juvenilní
parkinsonský syndrom
Ramsayův-Huntův syndrom paralýzy

 

Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinsonism
Autosomal Dominant Parkinsonism
Autosomal Recessive Juvenile Parkinson Disease
Autosomal Recessive Juvenile Parkinsonism
Autosomal Recessive Parkinsonism
Chromosome 6-Linked Autosomal Recessive Parkinsonism
Experimental Parkinson Disease
Experimental Parkinsonism
Experimental Parkinsonism, MPTP-Induced
Familial Juvenile Parkinsonism
Familial Parkinson Disease, Autosomal Recessive
Juvenile Parkinson Disease
Juvenile Parkinson Disease, Autosomal Dominant
Juvenile Parkinson Disease, Autosomal Recessive
Juvenile Parkinsonism, Autosomal Dominant
Juvenile Parkinsonism, Autosomal Recessive
MPTP-Induced Experimental Parkinsonism
Parkinson Disease 2
Parkinson Disease 2, Autosomal Recessive Juvenile
Parkinson Disease Autosomal Recessive, Early Onset
Parkinson Disease, Autosomal Dominant. Juvenile
Parkinson Disease, Experimental
Parkinson Disease, Familial, Autosomal Recessive
Parkinson Disease, Juvenile
Parkinson Disease, Juvenile, Autosomal Dominant
Parkinson Disease, Juvenile, Autosomal Recessive
Parkinsonian Diseases
Parkinsonian Syndrome
Parkinsonian Syndromes
Parkinsonism
Parkinsonism, Early Onset, with Diurnal Fluctuation
Parkinsonism, Early-Onset, With Diurnal Fluctuation
Parkinsonism, Experimental
Parkinsonism, Juvenile
Parkinsonism, Juvenile, Autosomal Dominant
Parkinsonism, Juvenile, Autosomal Recessive
Ramsay Hunt Paralysis Syndrome

Persistent link   https://www.medvik.cz/link/D020734
Definition

A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.

Annotation
Gen: prefer specifics; do not confuse entry term RAMSAY HUNT PARALYSIS SYNDROME with RAMSAY HUNT AURICULAR SYNDROME see HERPES ZOSTER OTICUS or RAMSAY HUNT CEREBELLAR SYNDROME see MYOCLONIC CEREBELLAR DYSSYNERGIA
DUI
D020734 MeSH Browser
CUI
M0328250
Previous indexing
Parkinson Disease (1966-1999)
History note
2000; for PARKINSONISM use PARKINSON DISEASE 1978-1999; for PARKINSONIAN SYNDROME use PARKINSON DISEASE, SECONDARY 1974-1999; for RAMSAY HUNT PARALYSIS SYNDROME use PARKINSON DISEASE 1992-1999
Public note
2000; for PARKINSONISM see PARKINSON DISEASE 1978-1999; for PARKINSONIAN SYNDROME see PARKINSON DISEASE, SECONDARY 1974-1999: for RAMSAY HUNT PARALYSIS SYNDROME see PARKINSON DISEASE 1992-1999

C Diseases
C10.228.140 Brain Diseases 1 178
C10.228.140.079 Basal Ganglia Diseases 100
C10.228.140.079.294 Chorea Gravidarum 2
C10.228.140.079.357 Dystonia Musculorum Deformans 3
C10.228.140.079.493 Hepatolenticular Degeneration 243
C10.228.140.079.545 Huntington Disease 322
C10.228.140.079.590 Meige Syndrome 9
C10.228.140.079.612 Multiple System Atrophy 56
C10.228.140.079.737 Neuroleptic Malignant Syndrome 46
C10.228.140.079.862 Parkinsonian Disorders 301
C10.228.140.079.862.400 Lewy Body Disease 115
C10.228.140.079.862.500 Parkinson Disease 1 580
C10.228.140.079.862.800 Parkinson Disease, Secondary 35
C10.228.140.079.882 Supranuclear Palsy, Progressive 50
C10.228.140.079.898 Tourette Syndrome 86
C10.228.662 Movement Disorders 914
C10.228.662.037 Akathisia, Drug-Induced 29
C10.228.662.075 Angelman Syndrome 35
C10.228.662.262 Dyskinesias 88
C10.228.662.300 Dystonic Disorders 81
C10.228.662.350 Essential Tremor 55
C10.228.662.550 Multiple System Atrophy 56
C10.228.662.600 Parkinsonian Disorders 301
C10.228.662.600.200 Lewy Body Disease 115
C10.228.662.600.400 Parkinson Disease 1 580
C10.228.662.600.700 Parkinson Disease, Secondary 35
C10.228.662.825 Tic Disorders 25

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