SEGAWA SINROME (CLINICAL CASE)

Ирода Камиловна РУСТАМОВА, Ойдин Бахрамовна КУЧКАРОВА, Сайера Акмалджановна КАСЫМОВА

Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research · 2021-yil

Annotatsiya

We examined a stationary patient who was admitted to the Department of Neurology 1 of ASMI Clinics with complaints of involuntary movements in the extremities, constriction in them, limitation of movements, involuntary turning of the neck and trunk in one direction. When prescribing levodopa drugs (madopar 125mg/day), in addition to the cyclodol (it was taken years ago) (4mg/day), noted that severity of motor symptoms significantly  decreased  on several days. Described features are specific in this syndrome. Segawa syndrome make it possible to distinquish it as an independent nasological unit and to correctly classify it as one of the diseases “dystonia-plus syndromes” at the moment.

Maqola ma’lumotlari
MualliflarИрода Камиловна РУСТАМОВА, Ойдин Бахрамовна КУЧКАРОВА, Сайера Акмалджановна КАСЫМОВА
JurnalЖурнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research
Nashr sanasi2021-06-23
Jild1
Son2
TilRus

Kalit so‘zlar

синдром Сегавы, наследственные дистонии, дофа-чувствительная дистония, торсионная дистония, Segawa syndrome, hereditary dystonia, dopamine responsive dystonia, torsion dostonia, Сегава синдром, ирсий дистонии, дофаминга сезгир дистония, торсион дистония

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