Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations.

doi:10.1016/j.parkreldis.2013.05.013

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Article

Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations.

Parkinsonism & related disorders - 1 Oct 2013

Sundal Christina, Fujioka Shinsuke, Van Gerpen Jay A, Wider Christian, Nicholson Alexandra M, Baker Matt, Shuster Elizabeth A, Aasly Jan, Spina Salvatore, Ghetti Bernardino, Roeber Sigrun, Garbern James, Tselis Alex, Swerdlow Russell H, Miller Bradley B, Borjesson-Hanson Anne, Uitti Ryan J, Ross Owen A, Stoessl A Jon, Rademakers Rosa, Josephs Keith A, Dickson Dennis W, Broderick Daniel, Wszolek Zbigniew K

Abstract excerpt

Atypical Parkinsonism associated with white matter pathology has been described in cerebrovascular diseases, mitochondrial cytopathies, osmotic demyelinating disorders, leukoencephalopathies leukodystrophies, and others. Hereditary diffuse leukoencephalopathy with spheroids (HDLS) is an autosomal dominant disorder with symptomatic onset in midlife and death within a few years after symptom onset. Neuroimaging...

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Identifiers

PMID: 23787135
DOI: 10.1016/j.parkreldis.2013.05.013
PMCID: PMC3977389

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