一种新型DLG4变体会导致DLG4相关性突触病和智力退化

IF 1 Q4 GENETICS & HEREDITY Human Genome Variation Pub Date : 2024-01-05 DOI:10.1038/s41439-023-00260-x
Sachi Tokunaga, Hideki Shimomura, Naoko Taniguchi, Kumiko Yanagi, Tadashi Kaname, Nobuhiko Okamoto, Yasuhiro Takeshima
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引用次数: 0

摘要

DLG4相关突触病是一种由DLG4变异体引起的神经发育障碍。我们在一名日本女孩身上发现了一个新的杂合换框变异体NM_001321075.3(DLG4):c.554_563del。她在两岁时出现智力退化,但没有运动迟缓,被诊断为自闭症谱系障碍和注意力缺陷/多动障碍。认识到智力倒退患者可能患有与DLG4相关的突触病,对于确保准确诊断非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A novel DLG4 variant causes DLG4-related synaptopathy with intellectual regression

DLG4-related synaptopathy is a neurodevelopmental disorder caused by a DLG4 variant. We identified a novel de novo heterozygous frameshift variant, NM_001321075.3(DLG4):c.554_563del, in a Japanese girl. Intellectual regression without motor delay was observed at 2 years of age, and she was diagnosed with autism spectrum disorder and attention-deficit/hyperactivity disorder. Recognizing the possibility of DLG4-related synaptopathy in patients with intellectual regression is important for ensuring an accurate diagnosis.

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来源期刊
Human Genome Variation
Human Genome Variation Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
13 weeks
期刊最新文献
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