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DeCS
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Descriptor English:
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Unverricht-Lundborg Syndrome
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Descriptor Spanish:
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Síndrome de Unverricht-Lundborg
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Descriptor Portuguese:
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Síndrome de Unverricht-Lundborg
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Synonyms English:
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Baltic Myoclonic Epilepsies
Baltic Myoclonic Epilepsy
Baltic Myoclonus
Baltic Myoclonus Epilepsies
Baltic Myoclonus Epilepsy
Disease, Unverricht
Disease, Unverricht-Lundborg
Diseases, Unverricht
Diseases, Unverricht-Lundborg
Epilepsies, Baltic Myoclonic
Epilepsies, Baltic Myoclonus
Epilepsy, Baltic Myoclonic
Epilepsy, Baltic Myoclonus
Epilepsy, Mediterranean Myoclonic
Epilepsy, Progressive Myoclonic 1
Epilepsy, Progressive Myoclonic 1a
Epilepsy, Progressive Myoclonic Type 1
Epilepsy, Progressive Myoclonus 1
Lundborg Unverricht Syndrome
Lundborg-Unverricht Syndrome
Mediterranean Myoclonic Epilepsy
Myoclonic Epilepsies, Baltic
Myoclonic Epilepsy of Unverricht and Lundborg
Myoclonic Epilepsy, Baltic
Myoclonic Epilepsy, Mediterranean
Myoclonus Epilepsies, Baltic
Myoclonus Epilepsy, Baltic
Myoclonus Progressive Epilepsy of Unverricht and Lundborg
Myoclonus, Baltic
Progressive Myoclonus Epilepsy 1
Progressive Myoclonus Epilepsybaltic Myoclonic Epilepsy
Syndrome, Lundborg-Unverricht
Syndrome, Unverricht-Lundborg
Unverricht Disease
Unverricht Diseases
Unverricht Lundborg Disease
Unverricht Lundborg Syndrome
Unverricht-Lundborg Disease
Unverricht-Lundborg Diseases
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Tree Number:
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C10.228.140.490.375.130.650.900
C10.228.140.490.493.063.650.900
C10.574.500.875
C16.320.400.940
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Definition English:
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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) |
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See Related English:
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Cystatin B
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History Note English:
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2000; for LUNDBORG-UNVERRICHT SYNDROME use EPILEPSY, MYOCLONIC 1977-1999
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Allowable Qualifiers English:
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Record Number:
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34276
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Unique Identifier:
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D020194
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Occurrence in VHL:
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Similar:
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DeCS
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