Parkinson Disease 8, Autosomal Dominant; Park8

Clinical Features

Top most frequent phenotypes and symptoms related to Parkinson Disease 8, Autosomal Dominant; Park8

  • Seizures
  • Cognitive impairment
  • Delayed speech and language development
  • Tremor
  • Dementia
  • Cerebral cortical atrophy
  • Rigidity
  • Mental deterioration
  • Postural instability
  • Parkinsonism

And another 21 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Parkinson Disease 8, Autosomal Dominant; Park8 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
LRRK2 DNA Sequencing Test.

By Athena Diagnostics Inc (United States).

LRRK2
Specificity
100 %
Genes
100 %
Complete Parkinsonism Evaluation.

By Athena Diagnostics Inc (United States).

SNCA, PINK1, PARK7, LRRK2, PRKN
Specificity
20 %
Genes
100 %
LRRK2 DNA Test.

By Athena Diagnostics Inc (United States).

LRRK2
Specificity
100 %
Genes
100 %
Movement Disorders Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).

SCP2, SGCE, SLC20A2, SLC2A1, SLC6A3, SNCA, SPR, SQSTM1, SUCLA2, SUOX, TAF1, TH, TIMM8A, TREX1, MCOLN1, VPS35, FBXO7, CACNA1A, NPC2, PINK1 , (...)

View the complete list with 72 more genes
Specificity
2 %
Genes
100 %
Parkinson's Disease.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).

SLC6A3, SNCA, TAF1, TH, VPS35, FBXO7, PINK1, PARK7, LRRK2, CSF1R, DCTN1, ATP13A2, GBA, GCH1, MAPT, ATP1A3, PRKN, PLA2G6, POLG
Specificity
6 %
Genes
100 %
LRRK2.

By Institute for Human Genetics University Clinic Freiburg (Germany).

LRRK2
Specificity
100 %
Genes
100 %
Detection of the G2019S mutation in exon 41 of the LRRK2 gene.

By Neurogenetics Department Cyprus Institute of Neurology and Genetics (Cyprus).

LRRK2
Specificity
100 %
Genes
100 %
LRRK2. Sequencing of the exons 31, 35 and 41.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

LRRK2
Specificity
100 %
Genes
100 %

You can get up to 45 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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