DYT13 gene related symptoms and diseases
All the information presented here about the DYT13 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to DYT13 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Tremor | Very Common - Between 80% and 100% cases |
| Blepharospasm | Very Common - Between 80% and 100% cases |
| Craniofacial dystonia | Very Common - Between 80% and 100% cases |
| Writer's cramp | Very Common - Between 80% and 100% cases |
| Oromandibular dystonia | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with DYT13 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Torsion dystonia
- Focal dystonia
- Action tremor
- Generalized dystonia
- Dystonia
- Limb dystonia
- Postural tremor
- Torticollis
And 5 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to DYT13 gene
Here you will find a list of rare diseases related to the DYT13. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
PRIMARY DYSTONIA, DYT13 TYPE
Alternate names
PRIMARY DYSTONIA, DYT13 TYPE Is also known as dyt13, primary dystonia with mixed phenotype, primary torsion dystonia with predominant craniocervical or upper limb onset
Description
DYT13 type primary dystonia is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement.
Most common symptoms of PRIMARY DYSTONIA, DYT13 TYPE
- Tremor
- Dystonia
- Postural instability
- Involuntary movements
- Stereotypy
More info about PRIMARY DYSTONIA, DYT13 TYPE
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