The aetiology and pathogenesis of Parkinson's disease (PD) remain unkn
own. There is a consensus emerging that there are likely to be multipl
e aetiologies that may result in the clinical and pathological abnorma
lities common to the majority of patients with idiopathic PD. Genetic
factors have been suggested as important in either the cause of PD or
in determining susceptibility. The recent linkage in one large pedigre
e of a gene for autosomal dominant parkinsonism to chromosome 4q21-23
and the subsequent identification of a mutation in the alpha-synuclein
gene of this region are important steps towards identifying a biochem
ical deficiency capable of causing selective dopaminergic cell death.
However, the relevance of such a defect to the majority of patients wi
th apparent sporadic PD remains to be established. Factors that may pr
edispose to substantia nigral cell loss, including mitochondrial dysfu
nction and oxidative damage, could be common to a number of separate a
etiologies. A better understanding of these and their relationship to
neuronal loss may provide further clues to aetiology.