Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research Volume 7 Issue 3 (2026)
CLINICAL CASE: AICARDI SYNDROME IN A MALE CHILD
Шамансурова Шаанвар Шамурадович, Охунбаев Жахонгир Музаффарович, Зиямухамедова Нилуфар Марҳаматовна
Abstract
Early childhood epileptic encephalopathies are among the most significant challenges in modern pediatric neurology. They are characterized by early onset of epileptic seizures and may contribute progressive psychomotor disfunction. Aicardi syndrome is one of the rare genetic disorder, which is characterized by a triad of symptoms: corpus callosum agenesis, infantile spasms and ophthalmological abnormalities. Despite the rarity of this condition, its study is of considerable scientific interest, particularly in the context of the limited number of reported clinical cases in the Republic of Uzbekistan
синдром Айкарди, инфантильные спазмы, агенезия мозолистого тела, эпилептическая энцефалопатия, микроцефалияAicardi syndrome, infantile spasms, corpus callosum agenesis, epileptic encephalopathy, microcephalyАйкарди синдроми, инфантил спазмлар, мия қадоқсимон танаси агенезияси, эпилептик энцефалопатия, микроцефалия
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