Search on: BIOTIN-RESPONSIVE ENCEPHALOPATHIES 
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Descriptor English:   Myoclonic Epilepsies, Progressive 
Descriptor Spanish:   Epilepsias Mioclónicas Progresivas 
Descriptor Portuguese:   Epilepsias Mioclônicas Progressivas 
Synonyms English:   Ataxia, Chorea, Seizures, And Dementia
Atypical Inclusion-Body Disease
Familial Progressive Myoclonic Epilepsy
Haw River Syndrome
Myoclonic Epilepsy, Progressive
Myoclonus-Nephropathy Syndrome
Naito Oyanagi Disease
Naito-Oyanagi Disease
Progressive Myoclonic Epilepsy
Progressive Myoclonus Epilepsies
Action Myoclonus Renal Failure Syndrome
Atrophies, Dentatorubral-Pallidoluysian
Atrophy, Dentatorubral-Pallidoluysian
Atypical Inclusion Body Disease
Atypical Inclusion-Body Diseases
Biotin Responsive Encephalopathy
Biotin-Responsive Encephalopathies
Dentatorubral Pallidoluysian Atrophy
Dentatorubral-Pallidoluysian Atrophies
Disease, Atypical Inclusion-Body
Disease, Naito-Oyanagi
Diseases, Atypical Inclusion-Body
Diseases, Naito-Oyanagi
Encephalopathies, Biotin-Responsive
Encephalopathy, Biotin-Responsive
Epilepsies, Progressive Myoclonic
Epilepsies, Progressive Myoclonus
Epilepsy, Progressive Myoclonic
Epilepsy, Progressive Myoclonus
Haw River Syndromes
Inclusion-Body Disease, Atypical
Inclusion-Body Diseases, Atypical
May White Syndrome
Myoclonus Epilepsies, Progressive
Myoclonus Nephropathy Syndrome
Myoclonus-Nephropathy Syndromes
Naito-Oyanagi Diseases
Oyanagi Disease, Naito
Progressive Myoclonic Epilepsies
Progressive Myoclonus Epilepsy
River Syndrome, Haw
River Syndromes, Haw
Syndrome, Haw River
Syndrome, Myoclonus-Nephropathy
Syndromes, Haw River
Syndromes, Myoclonus-Nephropathy
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 DG diagnostic imaging
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
RT radiotherapy RH rehabilitation
SU surgery TH therapy
UR urine VE veterinary
VI virology  
Record Number:   34274 
Unique Identifier:   D020191 

Occurrence in VHL:
 

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