Parkinson Disease 7, Autosomal Recessive Early-Onset

Alternative Names

  • PARK7
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WHO-ICD-10 version:2010

Diseases of the nervous system

Extrapyramidal and movement disorders

OMIM Number

606324

Mode of Inheritance

Autosomal recessive

Gene Map Locus

1p36

Description

PARK7 represents an early-onset (usually <40 years) form of Parkinson's disease caused by recessive mutations in the DJ1 gene; other subjects lacking mutations in DJ1 have exhibited homozygosity at markers adjacent to DJ1 locus. Patients exhibit asymmetric onset of symptoms including resting tremor, postural tremor, bradykinesia, and loss of postural reflexes.

Epidemiology in the Arab World

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Other Reports

Lebanon

Ibanez et al., 2003 described early onset autosomal recessive parkinsonism in 100 families (91 with multiple affected individuals, and 9 with single affecteds), 2 Lebanese families were among those diagnosed.  Haploidentity studies revealed homozygosity at locus marker D1S1612 which is adjacent to the DJ1 gene locus. 

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