Dohrn Maike F, Heller Corina, Zengeler Diana, Obermaier Carolin D, Biskup Saskia, Weis Joachim, Nikolin Stefan, Claeys Kristl G, Schöne Ulrike, Beijer Danique, Winter Natalie, Achenbach Pascal, Gess Burkhard, Schulz Jörg B, Mulahasanovic Lejla
Department of Neurology, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Dr. John T. Macdonald Foundation, Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, FL, USA.
Neurol Res Pract. 2022 Feb 1;4(1):5. doi: 10.1186/s42466-022-00169-w.
By whole-exome sequencing, we found the heterozygous POLG variant c.3542G>A; p.Ser1181Asn in a family of four affected individuals, presenting with a mixed neuro-myopathic phenotype. The variant is located within the active site of polymerase gamma, in a cluster region associated with an autosomal dominant inheritance. In adolescence, the index developed distal atrophies and weakness, sensory loss, afferent ataxia, double vision, and bilateral ptosis. One older sister presented with Charcot-Marie-Tooth-like symptoms, while the youngest sister and father reported exercise-induced muscle pain and proximal weakness. In none of the individuals, we observed any involvement of the central nervous system. Muscle biopsies obtained from the father and the older sister showed ragged-red fibers, and electron microscopy confirmed mitochondrial damage. We conclude that this novel POLG variant explains this family's phenotype.
通过全外显子组测序,我们在一个四口之家的四名患病个体中发现了杂合的POLG变异c.3542G>A;p.Ser1181Asn,他们表现出混合性神经肌肉病表型。该变异位于聚合酶γ的活性位点内,处于与常染色体显性遗传相关的簇区域。在青春期,先证者出现远端萎缩和无力、感觉丧失、传入性共济失调、复视和双侧上睑下垂。一位姐姐表现出类似夏科-马里-图斯病的症状,而最小的妹妹和父亲报告有运动诱发的肌肉疼痛和近端无力。在所有个体中,我们均未观察到中枢神经系统受累。从父亲和姐姐身上获取的肌肉活检显示有破碎红纤维,电子显微镜检查证实存在线粒体损伤。我们得出结论,这种新的POLG变异解释了该家庭的表型。