Duchenne muscular dystrophy is a severe genetically determined disease in which nervous system involvement extends far beyond neuromuscular pathology. The deficit of dystrophin protein in brain structures creates the neurobiological foundation for a spectrum of neurodevelopmental disorders, among which autistic disturbances occupy a special place. This article analyzes current understanding of the mechanisms of central nervous system involvement in this disease, the frequency and clinical manifestations of autism spectrum disorders, and the methodological challenges of their identification in patients with pronounced motor deficits. The necessity of concurrent application of neuropsychological and functional-motor scales in the diagnostic algorithm is substantiated.
| Mualliflar | Омонова Умида Тулкиновна, Зияходжаева Зилолахон Бахрамовна, Тилалова Улгузиой Йулдашевна |
|---|---|
| Jurnal | Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research |
| Nashr sanasi | 2026-05-15 |
| Jild | 7 |
| Son | 3 |
| Til | Rus |
миодистрофия Дюшенна, расстройство аутистического спектра, дистрофин, нейроразвитийные нарушения, когнитивный дефицит, диагностика, ADOS, M-CHAT, дети, Duchenne muscular dystrophy, autism spectrum disorder, dystrophin, neurodevelopmental disorders, cognitive deficit, diagnostics, ADOS, M-CHAT, children, Dyushenn miodistrofiyasi, autistik spektr buzilishi, distrofin, neyrorivoj buzilishlari, kognitiv defitsit, diagnostika, ADOS, M-CHAT, bolalar
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