Search on: UNVERRICHT-LUNDBORG SYNDROME 
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Descriptor English:   Unverricht-Lundborg Syndrome 
Descriptor Spanish:   Síndrome de Unverricht-Lundborg 
Descriptor Portuguese:   Síndrome de Unverricht-Lundborg 
Synonyms English:   Baltic Myoclonus
Lundborg-Unverricht Syndrome
Mediterranean Myoclonic Epilepsy  
Tree Number:   C10.228.140.490.250.650.900
C10.574.500.875
C16.320.400.940
Definition English:   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) 
History Note English:   2000; for LUNDBORG-UNVERRICHT SYNDROME use EPILEPSY, MYOCLONIC 1977-1999 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
congenital complications
diet therapy diagnosis
drug therapy economics
ethnology embryology
enzymology epidemiology
etiology genetics
history immunology
metabolism microbiology
mortality nursing
pathology prevention & control
physiopathology parasitology
psychology radiography
rehabilitation radionuclide imaging
radiotherapy surgery
therapy urine
ultrasonography veterinary
virology  
Record Number:   34276 
Unique Identifier:   D020194 

Occurrence in VHL:
 

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