Mallet Arellano A, Vergara M D, Kofman S, Espinosa A
Bol Med Hosp Infant Mex. 1978 Sep-Oct;35(5):813-21.
A five years old patient with myositis ossificans progressiva is presented. This very rare disease is inherited as an autosomal dominant and it is characterized by an abnormality of the connective tissue, specifically, aponeurosis, fascias, tendons and ligaments; the muscle are secondarly affected.
本文报告了一名患有进行性骨化性肌炎的5岁患者。这种极为罕见的疾病以常染色体显性方式遗传,其特征为结缔组织异常,具体表现为腱膜、筋膜、肌腱和韧带;肌肉随后受到影响。