Number of the records: 1
epilepsie myoklonické progresívne
Record number d020191 Date 06.06.2025 Type M Topical term epilepsie myoklonické progresívne Other term English (Pseudonym) Action Myoclonus-Renal Failure Syndrome
English (Pseudonym) Biotin-Responsive Encephalopathy
English (Pseudonym) Dentatorubral-Pallidoluysian Atrophy
English (Pseudonym) May-White Syndrome
Slovak (Pseudonym) Mayov-Whiteov syndróm
Slovak (Pseudonym) myoklonus akčný spojený so zlyhaním obličiek
Slovak (Pseudonym) myoklónia akčná spojená so zlyhaním obličiek
Slovak (Pseudonym) encefalopatia reagujúca na biotín
Slovak (Pseudonym) encefalopatia responzívna na biotín
Slovak (Pseudonym) atrofia dentátorubrálna-palidoluyziánska
UDC C10.228.140.490.375.130.650C10.228.140.490.493.063.650 Note A heterogeneous group of primarily familial EPILEPSY 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. 
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Number of the records: 1