MSTN gene related symptoms and diseases

All the information presented here about the MSTN gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,ORPHANET,HGNC, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to MSTN gene

Symptoms // Phenotype % Cases
Myoclonus Very Common - Between 80% and 100% cases
Skeletal muscle hypertrophy Very Common - Between 80% and 100% cases

Rare diseases associated to MSTN gene

Here you will find a list of rare diseases related to the MSTN. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


MYOSTATIN-RELATED MUSCLE HYPERTROPHY

Description

general increase in bulk of a muscle due to an increase in cell volume; it is not due to tumor formation, nor to an increase in the number of cells.

Most common symptoms of MYOSTATIN-RELATED MUSCLE HYPERTROPHY

  • Myoclonus
  • Skeletal muscle hypertrophy


More info about MYOSTATIN-RELATED MUSCLE HYPERTROPHY

SOURCES: OMIM ORPHANET


Potential gene panels for MSTN gene

Muscle hypertrophy (sequence analysis of MSTN gene) Panel

Portugal.

By CGC Genetics

This panel specifically test the MSTN gene.

More info about this panel
Portugal.

Muscle hypertrophy Panel

Germany.

By Centogene AG - the Rare Disease Company

This panel specifically test the MSTN gene.

More info about this panel
Germany.

Congenital and Distal Myopathies Panel Panel

Germany.

By CeGaT GmbH Congenital and Distal Myopathies Panel that also includes the following genes: RYR1 BIN1 STIM1 SUCLA2 TWNK TIA1 TK2 TNNT1 TPM2 TPM3

More info about this panel
Germany.

MSTN Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the MSTN gene.

More info about this panel
United States.

Myostatin-Related Muscle Hypertrophy: targeted gene sequencing Panel

Canada.

By CEN4GEN Institute for Genomics and Molecular Diagnostics

This panel specifically test the MSTN gene.

More info about this panel
Canada.

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