Novel homozygous frameshift variant in the ATCAY gene in an Iranian patient with Cayman cerebellar ataxia; expanding the neuroimaging and clinical features: a case report
Abstract Background Pathogenic variants in the ATCAY gene are associated with a rare autosomal recessive disorder called Cayman cerebellar ataxia. Affected individuals display psychomotor retardation, cerebellar dysfunction, nystagmus, intention tremor, ataxic gait and dysarthric in some cases. Case...
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Main Authors: | Elham Salehi Siavashani (Author), Mahmoud Reza Ashrafi (Author), Homa Ghabeli (Author), Morteza Heidari (Author), Masoud Garshasbi (Author) |
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Format: | Book |
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BMC,
2023-09-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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