Eurasian Journal of Medical and Natural Sciences 5-jild 10-son (2025) · 70–75-betlar

HEPATOCEREBRAL DEGENERATION: A CLINICAL CASE OF A RARE DISEASE

Bosimov, Muhammadzhon, Boboniyazov, Komilzhon

DOI: 10.5281/zenodo.17300093 · Manbada o'qish →

Annotatsiya

Hepatocerebral degeneration, also known as acquired hepatocerebral degeneration (AHD), is a rare neurological complication of chronic liver disease. It results from the accumulation of neurotoxic substances such as manganese and ammonia in the central nervous system, primarily affecting the basal ganglia. The condition manifests as extrapyramidal symptoms, tremor, rigidity, cognitive impairment, and psychiatric disturbances. This article presents a clinical case of a 52-year-old male with chronic liver cirrhosis who developed progressive neurological symptoms consistent with hepatocerebral degeneration. Diagnostic imaging, laboratory results, and therapeutic management are described. The report highlights the importance of early recognition and multidisciplinary treatment to prevent irreversible brain damage.

hepatocerebral degeneration, liver cirrhosis, manganese toxicity, basal ganglia, rare neurological disorder, Wilson-Konovalov disease, genetics, clinical presentation, diagnostics, treatment.гепатоцеребральная дегенерация, цирроз печени, интоксикация марганцем, базальные ганглии, редкое неврологическое заболевание, болезнь Вильсона-Коновалова, генетика, клиническая картина, диагностика, лечение.gepatoserebral degeneratsiya, jigar sirrozi, marganets toksikligi, bazal gangliyalar, kam uchraydigan nevrologik kasallik, Vilson-Konovalov kasalligi, genetika, klinik ko'rinish, diagnostika, davolash

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