Search on: PROGRESSIVE MYOCLONIC EPILEPSY, LAFORA TYPE 
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Descriptor English:   Lafora Disease 
Descriptor Spanish:   Enfermedad de Lafora 
Descriptor Portuguese:   Doença de Lafora 
Synonyms English:   Epilepsy, Progressive Myoclonic, Lafora
Progressive Myoclonic Epilepsy, Lafora Type  
Tree Number:   C10.228.140.490.250.650.500
C10.574.500.529
C16.320.400.480
Definition English:   A form of stimulus sensitive myoclonic epilepsy inherited as an autosomal recessive condition. The most common presenting feature is a single seizure in the second decade of life. This is followed by progressive myoclonus, myoclonic seizures, tonic-clonic seizures, focal occipital seizures, intellectual decline, and severe motor and coordination impairments. Most affected individuals do not live past the age of 25 years. Concentric amyloid (Lafora) bodies are found in neurons, liver, skin, bone, and muscle (From Menkes, Textbook of Childhood Neurology, 5th ed, pp111-110) 
History Note English:   2000; 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:   34275 
Unique Identifier:   D020192 

Occurrence in VHL:
 

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