The girl born after prenatal gene diagnosis carried a 9.4Kb fragment by PERT 87-15 and her serum CK level reached to 265U/L,otherwise her growth development was normal. Duchenne muscular dystrophy(DMD)or a carrier with DMD symptoms can be ruled out.

 
  • 产前基因诊断女孩携有 87-15的 9.;4Kb片段;CK2 6 5U /L;是杜氏肌营养不良症(DMD)致病基因携带者;现生长发育正常;排除她不是Duchenne(DMD)型肌营养不良症患者或有症状的DMD的女性携带者。
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