Work

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations

Year: 2001
Type: article
Study design: Case Report
Abstract: A Dutch family with autosomal recessive early-onset parkinsonism showed a heterozygous missense mutation in combination with a heterozygous exon deletion in the parkin gene. Although the main clinical syndrome consisted of parkinsonism, the proband clinically had additional mild gait ataxia and pathologically showed neuronal loss in parts of the spinocerebellar system, in addition to selective loss of dopaminergic neurons in the substantia nigra pars compacta. Lewy bodies and neurofibrillary tangles were absent, but tau pathology was found.
Source: Neurology
Language: English
Subfield: Neurology
Field: Medicine
Open Access status: green
OpenAlex ID: W2133865158
FWCI: 17.97
Cites: 11
Cited by: 253
Related to: 10