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Facio-scapulo-humeral muscular dystrophy with early joint contractures and rigid spine

机译:面肩肱肱肌营养不良伴早期关节挛缩和刚性脊柱

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摘要

Early joint contractures in childhood or adolescence irrespective of muscle weakness are usually found in Emery-Dreifuss muscular dystrophy and collagen-VI related diseases and only rarely in the early stages of other progressive muscular dystrophies. We report a patient presenting severe elbow contractures and a rigid-spine since his early childhood without any evident muscle weakness, who was diagnosed with facioscapulohumeral muscular dystrophy later in life. This case is interesting since there has been no report, to date, of patients with a phenotype resembling facioscapulohumeral muscular dystrophy also in association with early and prominent elbow contractures and spinal rigidity, since childhood, resembling Emery-Dreifuss muscular dystrophy. Our case further confirmed the phenotypic variability often observed in carriers of D4Z4 reduce allele, and highlights the complexity of a definitive diagnosis in these cases.
机译:儿童或青春期早期的关节挛缩症与肌肉无力无关,通常见于Emery-Dreifuss肌营养不良症和胶原VI相关疾病,很少见于其他进行性肌营养不良的早期。我们报道了一名患者,自幼年以来就出现了严重的肘关节挛缩和僵硬的脊柱,没有明显的肌肉无力,该患者后来被诊断为肩cap肱骨肌营养不良。该病例很有趣,因为迄今为止,尚无关于表皮相似的肩cap肱肌营养不良症的表型的报道,并且自童年以来还伴有早期和突出的肘关节挛缩和脊柱僵硬,类似于埃默里-德雷福斯的肌肉营养不良症。我们的病例进一步证实了在D4Z4携带者减少等位基因中经常观察到的表型变异,并突出了这些病例中明确诊断的复杂性。

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