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:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DH diet therapy
DT drug therapy 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 RA radiography
RI radionuclide imaging RT radiotherapy
RH rehabilitation SU surgery
TH therapy US ultrasonography
UR urine VE veterinary
VI virology  
Record Number:   34276 
Unique Identifier:   D020194 

Occurrence in VHL:
 

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