Atypical Presentations of Huntington Disease‐like 2 in South African Individuals

Background Huntington disease‐like 2 (HDL2) is a neurodegenerative disorder, affecting only individuals of African ancestry. Full penetrance occurs in individuals with 40 repeats or more. Objective To describe the phenotypic variability of HDL2 in a group of mixed ancestry individuals from South Afr...

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Veröffentlicht in:	Movement disorders clinical practice (Hoboken, N.J.) N.J.), 2024-07, Vol.11 (7), p.850-854
Hauptverfasser:	Narotam‐Jeena, Heena, Guttman, Mark, Hillegondsberg, Ludo, Coller, Riaan, Krause, Amanda, Carr, Jonathan
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Aged Black People - genetics Brain - diagnostic imaging Brain - pathology Brief Report chorea Chorea - diagnosis Chorea - genetics Cognition Disorders Dementia Female HDL2 Heredodegenerative Disorders, Nervous System - diagnosis Heredodegenerative Disorders, Nervous System - genetics Humans Huntington Huntington Disease - diagnosis Huntington Disease - ethnology Huntington Disease - genetics Huntingtons disease Magnetic Resonance Imaging Male Middle Aged Neurodegenerative Diseases - diagnosis Neurodegenerative Diseases - genetics Neurodegenerative Diseases - pathology South Africa - epidemiology
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