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Glial response in the midcingulate cortex in Huntington’s disease
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作者 Thulani H.Palpagama Andrea Kwakowsky 《Neural Regeneration Research》 SCIE CAS 2025年第1期207-208,共2页
Huntington’s disease(HD)is a genetic disease characterized by the progressive degeneration of the striatum and cortex.Patients can present with a variety of symptoms that can broadly be classified into motor symptoms... Huntington’s disease(HD)is a genetic disease characterized by the progressive degeneration of the striatum and cortex.Patients can present with a variety of symptoms that can broadly be classified into motor symptoms,inclusive of choreatic movements and rigidity,mood and psychiatric symptoms,such as depression and apathy,and cognitive symptoms,such as cognitive decline.The causal mutation underlying HD results from an expansion of a CAG repeat sequence on the IT15 gene,resulting in the formation and accumulation of a mutant huntingtin protein. 展开更多
关键词 HUNTINGTON DEGENERATION CORTEX
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Neuroinflammation as a therapeutic target in Huntington's disease
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作者 Andrea Kwakowsky Thulani H.Palpagama 《Neural Regeneration Research》 SCIE CAS 2025年第3期817-818,共2页
In 1872, George Huntington presented his essay “On Chorea” to the Meigs and Mason Academy of Medicine and, in doing so, detailed a disease that would later bear his name. Huntington's disease(HD) is a genetic, n... In 1872, George Huntington presented his essay “On Chorea” to the Meigs and Mason Academy of Medicine and, in doing so, detailed a disease that would later bear his name. Huntington's disease(HD) is a genetic, neurodegenerative disease that manifests as the loss of motor control,cognitive impairment,and mood and psychiatric changes in paents. 展开更多
关键词 HUNTINGTON INFLAMMATION MEDICINE
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