[Pitt-Hopkins syndrome caused by TCF4 gene novel mutation in a child].

Abstract excerpt

患儿 女，1岁5月龄，因“发现智力运动发育落后1年余”就诊。患儿表现为特异性面部特征与全面性发育迟缓，基因检测提示TCF4基因新发错义变异c.1739G>T（p.Arg580Leu），结合表型诊断为皮特-霍普金斯综合征。皮特-霍普金斯综合征是1种全球罕见的神经发育障碍疾病，该病尚无特效疗法，以个体化康复功能训练为主。.

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