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ATP7A基因新发变异致Menkes病1例

A case of Menkes disease caused by a novel ATP7A gene variation
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摘要 收集2020年12月深圳市儿童医院收治的1例ATP7A基因新发变异所致Menkes病患者的临床资料,回顾性分析其临床特征及基因变异特点。该例患儿的临床特征包括早发性癫痫,特殊面容,脑软化、萎缩,硬膜下积液,高乳酸血症,血铜降低;基因检测结果显示X染色体上ATP7A基因5号外显子存在半合子变异:c.1435C>T(p.Gln479Ter)。
作者 石晓萌 路新国 SHI Xiaomeng;LU Xinguo
出处 《中国医科大学学报》 CAS CSCD 北大核心 2021年第12期1141-1145,共5页 Journal of China Medical University
基金 深圳市医疗卫生三名工程(SZSM201812005) 深圳市医学重点学科建设项目(SZXK033) 广东省高水平临床重点专科项目(SZGSP012)。
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