共济失调
痉挛
复合杂合度
小脑共济失调
表型
运动障碍
等位基因
医学
外显子组测序
遗传学
生物
内科学
疾病
物理疗法
基因
精神科
作者
Isabell Cordts,Luisa Semmler,Jannik Prasuhn,Annette Seibt,Diran Herebıan,Tharsini Navaratnarajah,Joohyun Park,Natalie Deininger,Lucia Laugwitz,Sophia Göricke,Paul Lingor,Norbert Brüggemann,Alexander Münchau,Matthis Synofzik,Dagmar Timmann,Johannes A. Mayr,Tobias B. Haack,Felix Distelmaier,Marcus Deschauer
摘要
BACKGROUND: deficiency leads to an early-onset mitochondrial multi-organ disorder. METHODS: In-house exome and genome datasets (n = 14,303) were screened for patients with bi-allelic variants in COQ4. Work-up included clinical characterization and functional studies in patient-derived cell lines. RESULTS: concentrations, and elevated levels of the metabolic intermediate 6-demethoxyubiquinone. CONCLUSION: We report bi-allelic variants in COQ4 causing an adult-onset ataxia-spasticity spectrum phenotype and a disease course much milder than previously reported. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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