Search on: DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY 
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Descriptor English:   Myoclonic Epilepsies, Progressive 
Descriptor Spanish:   Epilepsias Mioclónicas Progresivas 
Descriptor Portuguese:   Epilepsias Mioclônicas Progressivas 
Synonyms English:   Action Myoclonus-Renal Failure Syndrome
Biotin-Responsive Encephalopathy
Dentatorubral-Pallidoluysian Atrophy
May-White Syndrome  
Tree Number:   C10.228.140.490.250.650
Definition English:   A heterogeneous group of primarily familial disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME. 
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:   34274 
Unique Identifier:   D020191 

Occurrence in VHL:
 

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