Department of Neurology, University Medical Center Schleswig-Holstein, Kiel, Germany.
Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Neurogenetics. 2023 Oct;24(4):273-278. doi: 10.1007/s10048-023-00728-6. Epub 2023 Aug 17.
Both, recessive (LGMD R1) and dominant (LGMD D4) inheritance occur in calpain 3-related muscular dystrophy. We report a family with calpain-related muscular dystrophy caused by two known variants in the calpain 3 gene (CAPN3, NM_000070.3; (I) c.700G>A, p.Gly234Arg and (II) c.1746-20C>G, p.?). Three family members are compound heterozygous and exhibit a relatively homogeneous phenotype characterized by progressive proximal weakness starting in the third to fourth decade of life in the shoulder girdle and spreading to the legs. Two family members affected only by the p.Gly234Arg heterozygous missense variants show a different phenotype characterized by severe exertional myalgia without overt pareses. We conclude that in our family, the missense variant causes a severe myalgic phenotype without pareses that is aggravated by the second intronic variant and put these findings in the context of previous studies of the same variants.
隐性(LGMD R1)和显性(LGMD D4)遗传均发生在钙蛋白酶 3 相关肌营养不良症中。我们报告了一个由钙蛋白酶 3 基因(CAPN3,NM_000070.3;(I)c.700G>A,p.Gly234Arg 和(II)c.1746-20C>G,p.?)中的两个已知变异引起的钙蛋白酶相关肌营养不良症家族。三个家族成员为复合杂合子,并表现出相对同质的表型,特征为肩部和腿部的近端进行性无力,始于第三至第四十年。受 p.Gly234Arg 杂合错义变异影响的两个家族成员表现出不同的表型,其特征为严重的劳累性肌痛而无明显的瘫痪。我们得出结论,在我们的家族中,错义变异导致无瘫痪的严重肌痛表型,第二个内含子变异使其加重,并将这些发现置于同一变异的先前研究背景下。