Morse R P, Rosman N P
Department of Pediatrics, Floating Hospital for Children, New England Medical Center Hospitals, Boston, Massachusetts 02111.
J Pediatr. 1993 Feb;122(2):254-6. doi: 10.1016/s0022-3476(06)80126-5.
We report our experience with four children, including one girl, in whom the eventual diagnosis of muscular dystrophy was made because of persistent, unexplained elevated serum aminotransferase values. Measurement of serum creatine kinase activity and careful physical examination are the most useful and cost-effective means of correctly identifying these patients.
我们报告了4名儿童（包括1名女孩）的情况，他们最终被诊断为肌肉萎缩症，原因是血清转氨酶值持续不明原因升高。测量血清肌酸激酶活性和仔细的体格检查是正确识别这些患者最有用且最具成本效益的方法。
