A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia
Kishin Koh, Haruo Shimazaki, Matsuo Ogawa and 1 more
Human Genome Variation · 2022
doi:10.1038/s41439-022-00204-x (opens in a new tab)
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Abstract
Abstract A heterozygous mutation in GRID2 that causes SCAR18 was first reported in an Algerian family with autosomal dominant cerebellar ataxia (ADCA). We identified the second ADCA family with a heterozygous GRID2 mutation. The Algerian family had cognitive impairment and hearing loss associated with cerebellar ataxia. However, the Japanese family presented here showed pure cerebellar ataxia. Therefore, we should also screen for the GRID2 mutation in ADCA families with pure cerebellar ataxia.
Abstract licence: CC BY
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