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Qualquer doença neurodegenerativa com coreia em que a causa da doença seja uma mutação no gene PRNP.
Nenhum ensaio clínico registrado para esta condição.
Huntington's disease phenocopy syndromes revisited: a clinical comparison and next-generation sequencing exploration.
Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?
A novel non-rapid-eye movement and rapid-eye-movement parasomnia with sleep breathing disorder associated with antibodies to IgLON5: a case series, characterisation of the antigen, and post-mortem study.
Huntington's disease and Huntington's disease-like syndromes: an overview.
The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician.