SLC35A2基因新生变异致先天性糖基化障碍1例

Chinese Journal of Neurology(2022)

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Abstract
先天性糖基化障碍(CDG)是一组累及多器官系统的遗传代谢性疾病,相对罕见。我院收治1例SLC35A2基因相关CDG患者,临床表现为成串痉挛发作、发育迟缓、多发畸形等。家系3人全外显子基因组测序发现SLC35A2基因新生杂合错义变异:c.844G>A(p.Gly282Arg),根据美国医学遗传学与基因组学学会指南预测为可能致病性突变。此位点国内尚未见报道。
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Key words
Congenital disorder of glycosylation,SLC35A2 gene,Epileptic encephalopathy,de novo Variant
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