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They can direct you to research, resources, and services. Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, oculomotor disorders, peripheral neuropathy, and ataxia of the gait, stance, and limbs due to cerebellar dysfunction. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.Living with a genetic or rare disease can impact the daily lives of patients and families. Spinocerebellar ataxia 5 (SCA5) is one of the many spinocerebellar ataxias, … Carbidopa. Spinocerebellar ataxia type 6 (SCA6) is a neurological condition characterized … Clinically, it is characterized by pure cerebellar dysfunction, slowly progressive unsteadiness of gait and stance, slurred speech, and abnormal eye movements with late onset. If you have questions about getting a diagnosis, you should contact a healthcare professional.If you can’t find a specialist in your local area, try contacting national or international specialists. When anticipation is observed in SCA36, the mutation is most often passed down from the affected father. You may want to review these resources with a medical professional.If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. If you do not want your question posted, please let us know.Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. OT = occupational therapist/therapy; PT = physical therapist/therapyRecommended Evaluations Following Initial Diagnosis in Individuals with Spinocerebellar Ataxia Type 6Basal ganglia signs, such as dystonia and blepharospasm, are noted in up to 25% of individuals.In a family with an established diagnosis of SCA6, it is appropriate to consider testing of symptomatic individuals regardless of age.Allelic Autosomal Dominant Disorders to Consider in the Differential Diagnosis of Spinocerebellar Ataxia Type 6Features of Spinocerebellar Ataxia Type 6Spinocerebellar Ataxia Type 6: Genes and DatabasesMolecular Genetic Testing Used in Spinocerebellar Ataxia Type 6Although the disease rarely manifests during years of fertility, measures to support imbalance should be enhanced in symptomatic pregnant women.Formal diagnostic criteria for spinocerebellar ataxia type 6 (SCA6) have not been established.The growing interest in cannabidiol (CBD) requires further empiric experience or clinical trials.Adam MP, Ardinger HH, Pagon RA, et al., editors. Eighty MSA patients were enrolled in our study; blood samples were collected and genetic screening of the familial case for known SCA loci was performed. GeneReviews® [Internet]. Please note that the table may not include all the possible conditions related to this disease.Making a diagnosis for a genetic or rare disease can often be challenging.