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Diagnosis information
Core diagnostic criteria, specifiers, differential considerations, and documentation support in one open, scan-friendly view.
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Core criterion A
Criteria met for major or mild NCD
Core criterion B
Insidious onset and gradual progression
Core criterion C
Clinically established Huntington's disease or at-risk with positive genetic testing
Core criterion D
Disturbance not better explained by another condition
Consistent with [Neurocognitive Disorder Due to Huntington's Disease] [specifier(s)]. In the context of genetically confirmed or clinically established Huntington's disease, there have been impairments in attention; impairments in executive functioning; impairments in learning and memory; impairments in language; impairments in perceptual-motor abilities; impairments in social cognition, forming a pattern meeting the threshold for a neurocognitive disorder. The presentation is further characterised by insidious onset and gradual progression; cognitive decline occurring in association with characteristic motor features such as chorea, dystonia, gait disturbance, slowed voluntary movements; emotional or behavioural changes such as irritability, depression, apathy, impulsivity, consistent with the neurodegenerative course of Huntington's disease. These symptoms have resulted in clinically significant impairment in social, occupational, or adaptive functioning.
Adapt this supplied template to the assessment. It is not a substitute for diagnostic reasoning or local documentation requirements.