揭露MYH2相关的肌肉病变:从病例系列和系统审查中获得的组织学遗传洞察力

Beatrice Labella1, Guy Brochier1,2, Maud Beuvin1

  • 1Neuromuscular Morphology Unit, Myology Institute, Groupe Hospitalier Universitaire Pitié-Salpêtrière, Paris, France.

PubMed
概括

在MYH2基因的致病变体导致先天性肌肉病变. 这项研究确定了新的MYH2变异,并突出了不同的临床表现,强调了医生对这种罕见的肌肉疾病提高认识的必要性.

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