Multiple System Atrophy, Parkinsonian Type

Description

Multiple system atrophy, parkinsonian type (MSA-p) is a form of multiple system atrophy (MSA; see this term) with predominant parkinsonian features (bradykinesia, rigidity, irregular jerky postural tremor, and postural instability).

Clinical Features

Top most frequent phenotypes and symptoms related to Multiple System Atrophy, Parkinsonian Type

  • Dysarthria
  • Depressivity
  • Constipation
  • Gait ataxia
  • Rigidity
  • Anxiety
  • Abnormal pyramidal sign
  • Postural instability
  • Parkinsonism
  • Progressive cerebellar ataxia

And another 20 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

Incidence and onset information

— Based on the latest data available Multiple System Atrophy, Parkinsonian Type have a estimated prevalence of 2.4 per 100k worldwide.
No data available about the known clinical features onset.

Alternative names

Multiple System Atrophy, Parkinsonian Type Is also known as msa-p, msa, parkinsonian type.

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.


Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Multiple System Atrophy, Parkinsonian Type Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMetĀ®Plus aCGH Analysis.

By Baylor Miraca Genetics Laboratories (United States).

RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB , (...)

View the complete list with 612 more genes
Specificity
1 %
Genes
100 %
COQ2 Sequence Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories (United States).

COQ2
Specificity
100 %
Genes
100 %
COQ2 Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

COQ2
Specificity
100 %
Genes
100 %
COQ2 Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

COQ2
Specificity
100 %
Genes
100 %
COQ2 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

COQ2
Specificity
100 %
Genes
100 %
Comprehensive Mitochondrial Metabolic Panel.

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

BCS1L, SCO1, SCO2, SDHB, SDHC, SDHD, SLC22A5, SLC25A13, SLC25A15, SLC25A3, SLC25A4, BTD, SUCLA2, SUCLG1, SURF1, TAZ, TWNK, TCN2, TFAM, TIMM8A , (...)

View the complete list with 173 more genes
Specificity
1 %
Genes
100 %
Ataxia Exome Panel.

By Genetic Services Laboratory University of Chicago (United States).

BCS1L, RTN2, SACS, SCN1A, SCN2A, SCN8A, SCO1, SDHA, SDHD, SLC16A2, SLC17A5, SLC19A2, SLC1A3, SLC20A2, SLC2A1, SLC6A1, SLC9A1, SLC9A6, SNAP25, SOD1 , (...)

View the complete list with 457 more genes
Specificity
1 %
Genes
100 %
Mitochondrial Disorders Panel (mtDNA Sequencing, Nuclear Genes Sequencing, and Deletion/Duplication).

By ARUP Laboratories, Molecular Genetics and Genomics (United States).

BCS1L, SCO1, SCO2, SDHB, SDHC, SDHD, SLC22A5, SLC25A13, SLC25A15, SLC25A3, SLC25A4, SLC3A1, SPG7, SUCLA2, SUCLG1, SUOX, SURF1, TAZ, TWNK, TIMM8A , (...)

View the complete list with 130 more genes
Specificity
1 %
Genes
100 %

We have 74 more panels available in our App

Get the app

Sources and references

You can check the following sources for additional information.

ORPHANET Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like VOHWINKEL SYNDROME; VOWNKL SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2; ICF2 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5 GLASS SYNDROME; GLASS CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more