We compared the clinical and neurological picture of hereditary spastic paraplegia (HSP) and cerebral palsy of spastic diplegia. The results of a neurological examination indicate that in patients in the comparison group, clinical symptoms, especially changes in the cranial innervation and motor sphere, were more pronounced compared to the main group. During a clinical and neurological examination of patients with HSP, we identified both pure spastic paraplegia, characterized only by motor disorders (71.5%), and spastic paraplegia with complications (20%) in the form of dysfunction of the cranial nerves, intellectual impairment of varying degrees (5.4%), pelvic organ dysfunction (4.4%), history of seizures (5.2%), polyneuropathies (3.15%), extraneural symptoms were detected in 3 (3.1%) patients, i.e. congenital skin changes in the form of ichthyosis.
| Mualliflar | Омонова Умида Тулкиновна, Окилжонова Нигорахон Абдулазизовна, Бахромова Гавхар Акмаловна |
|---|---|
| Jurnal | Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research |
| Nashr sanasi | 2024-05-27 |
| Jild | 5 |
| Son | 2 |
| Til | Rus |
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