MYOCLONIC DYSTONIA SYNDROME IN CHILDREN

Гулямова Дурдона Насриддиновна

Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research · 2024-yil

Annotatsiya

Myoclonic dystonia is a genetically heterogeneous condition that leads to impaired muscle function (myoclonic hyperkinesis), as well as dystonia of the musculature of the upper body – neck, upper limb girdle. The symptoms of this condition are sharp muscle twitches (arms, neck, occasionally legs), especially when performing subtle movements. Then dystonia joins, which can manifest itself with a torticollis and an unusual posture of the patient. The diagnosis of myoclonic dystonia is based on the data of the patient's current status and molecular genetic analysis.

Maqola ma’lumotlari
MualliflarГулямова Дурдона Насриддиновна
JurnalЖурнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research
Nashr sanasi2024-03-30
Jild5
Son1
TilRus

Kalit so‘zlar

дистония; миоклонус; мышечные подергивания; мутация ε-саркогликана, dystonia; myoclonus; muscle twitching; e-sarcoglycan mutation, дистония; миоклонус; мушакларнинг тортишиши; ε-саркогликан мутацияси

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