SCA25 gene related symptoms and diseases

All the information presented here about the SCA25 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to SCA25 gene

Symptoms // Phenotype	% Cases
Scoliosis	Very Common - Between 80% and 100% cases
Urinary urgency	Very Common - Between 80% and 100% cases
Facial tics	Very Common - Between 80% and 100% cases
Abolished vibration sense	Very Common - Between 80% and 100% cases
Impaired distal tactile sensation	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with SCA25 gene alterations may also develop some of the following symptoms and phenotypes:

• Commonly - More than 50% cases

• Facial myokymia
• Diffuse cerebellar atrophy
• Decreased number of large peripheral myelinated nerve fibers
• Spastic dysarthria
• Areflexia of lower limbs
• Tics
• EMG: neuropathic changes
• Episodic abdominal pain

And 19 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to SCA25 gene

Here you will find a list of rare diseases related to the SCA25. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

Search interest in SCA25

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