Unverricht-Lundborg Syndrome [Unverrichtův-Lundborgův syndrom]

topical
1
Terms

Baltický myoklonus
středomořská myoklonická epilepsie

 

Baltic Myoclonic Epilepsy
Baltic Myoclonus
Baltic Myoclonus Epilepsy
Epilepsy, Progressive Myoclonic 1
Epilepsy, Progressive Myoclonic 1a
Epilepsy, Progressive Myoclonic Type 1
Epilepsy, Progressive Myoclonus 1
Lundborg-Unverricht Syndrome
Mediterranean Myoclonic Epilepsy
Myoclonic Epilepsy of Unverricht and Lundborg
Myoclonus Progressive Epilepsy of Unverricht and Lundborg
Progressive Myoclonus Epilepsy 1
Progressive Myoclonus Epilepsybaltic Myoclonic Epilepsy
Unverricht Disease
Unverricht-Lundborg Disease

Persistent link   https://www.medvik.cz/link/D020194
Definition

An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, DYSARTHRIA, and intention tremor. Myoclonic seizures are severe and continuous, and tend to be triggered by movement, stress, and sensory stimuli. The age of onset is between 8 and 13 years, and the condition is relatively frequent in the Baltic region, especially Finland. (From Menkes, Textbook of Child Neurology, 5th ed, pp109-110)

DUI
D020194 MeSH Browser
CUI
M0328656
Previous indexing
Epilepsies, Myoclonic (1977-1999); Epilepsy (1965-1976); Myoclonus (1965-1976)
History note
2000; for LUNDBORG-UNVERRICHT SYNDROME use EPILEPSY, MYOCLONIC 1977-1999
Public note
2000; for LUNDBORG-UNVERRICHT SYNDROME see EPILEPSY, MYOCLONIC 1977-1999

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 1
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 1
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C10 Nervous System Diseases 1 878
C10.228 Central Nervous System Diseases 808
C10.228.140 Brain Diseases 1 178
C10.228.140.490 Epilepsy 3 247
C10.228.140.490.375 Epilepsy, Generalized 58
C10.228.140.490.375.130 Epilepsies, Myoclonic 45
C10.228.140.490.375.130.650 Myoclonic Epilepsies, Progressive 10
C10.228.140.490.375.130.650.500 Lafora Disease 1
C10.228.140.490.375.130.650.700 MERRF Syndrome 4
C10.228.140.490.375.130.650.900 Unverricht-Lundborg Syndrome 1
C10.228.140.490.493 Epileptic Syndromes 19
C10.228.140.490.493.063 Epilepsies, Myoclonic 45
C10.228.140.490.493.063.650 Myoclonic Epilepsies, Progressive 10
C10.228.140.490.493.063.650.500 Lafora Disease 1
C10.228.140.490.493.063.650.700 MERRF Syndrome 4
C10.228.140.490.493.063.650.900 Unverricht-Lundborg Syndrome 1
C10.574 Neurodegenerative Diseases 641
C10.574.500 Heredodegenerative Disorders, Nervous System 45
C10.574.500.024 Alexander Disease 6
C10.574.500.050 Amyloid Neuropathies, Familial 20
C10.574.500.175 Bulbo-Spinal Atrophy, X-Linked 8
C10.574.500.300 Canavan Disease 9
C10.574.500.362 Cockayne Syndrome 4
C10.574.500.393 Dystonia Musculorum Deformans 3
C10.574.500.425 Gerstmann-Straussler-Scheinker Disease 22
C10.574.500.487 Hepatolenticular Degeneration 243
C10.574.500.490 Hereditary Central Nervous System Demyelinating Diseases 11
C10.574.500.493 Hereditary Sensory and Autonomic Neuropathies 26
C10.574.500.495 Hereditary Sensory and Motor Neuropathy 71
C10.574.500.497 Huntington Disease 322
C10.574.500.529 Lafora Disease 1
C10.574.500.545 Myotonia Congenita 17
C10.574.500.547 Myotonic Dystrophy 94
C10.574.500.549 Neurofibromatoses 28
C10.574.500.550 Neuronal Ceroid-Lipofuscinoses 29
C10.574.500.662 Optic Atrophies, Hereditary 5
C10.574.500.700 Pantothenate Kinase-Associated Neurodegeneration 17
C10.574.500.812 Spinal Muscular Atrophies of Childhood 59
C10.574.500.825 Spinocerebellar Degenerations 30
C10.574.500.850 Tourette Syndrome 86
C10.574.500.865 Tuberous Sclerosis 141
C10.574.500.875 Unverricht-Lundborg Syndrome 1
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.400.024 Alexander Disease 6
C16.320.400.050 Amyloid Neuropathies, Familial 20
C16.320.400.100 Bulbo-Spinal Atrophy, X-Linked 8
C16.320.400.150 Canavan Disease 9
C16.320.400.200 Cockayne Syndrome 4
C16.320.400.330 Dystonia Musculorum Deformans 3
C16.320.400.350 Gerstmann-Straussler-Scheinker Disease 22
C16.320.400.361 Hepatolenticular Degeneration 243
C16.320.400.367 Hereditary Central Nervous System Demyelinating Diseases 11
C16.320.400.375 Hereditary Sensory and Motor Neuropathy 71
C16.320.400.415 Hereditary Sensory and Autonomic Neuropathies 26
C16.320.400.430 Huntington Disease 322
C16.320.400.480 Lafora Disease 1
C16.320.400.525 X-Linked Intellectual Disability 17
C16.320.400.540 Myotonia Congenita 17
C16.320.400.542 Myotonic Dystrophy 94
C16.320.400.550 Neuroacanthocytosis 6
C16.320.400.560 Neurofibromatoses 28
C16.320.400.600 Neuronal Ceroid-Lipofuscinoses 29
C16.320.400.630 Optic Atrophies, Hereditary 5
C16.320.400.650 Pantothenate Kinase-Associated Neurodegeneration 17
C16.320.400.765 Spinal Muscular Atrophies of Childhood 59
C16.320.400.780 Spinocerebellar Degenerations 30
C16.320.400.820 Tourette Syndrome 86
C16.320.400.880 Tuberous Sclerosis 141
C16.320.400.940 Unverricht-Lundborg Syndrome 1

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