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1。具有一级或二级亲戚，对Duchenne或Becker肌肉营养不良的临床诊断。xxiii。dmd测序和/或缺失/重复分析（0218U，81161，81408）为所有其他适应症的研究都考虑了诊断Duchenne肌肉营养不良（DMD）或Becker肌肉营养不良（BMD）的诊断。facioscapulohumeral肌肉营养不良（FSHD）D4Z4单倍型分析和/或SMCHD1和DNMT3B测序和/或缺失/重复分析或Multigene Banel XXIV。D4Z4 haplotype analysis (81404), and/or SMCHD1 (81479) and DNMT3B (81479) sequencing and/or deletion/duplication analysis or multigene panel analysis (81404, 81479) to establish or confirm a diagnosis of facioscapulohumeral muscular dystrophy may be considered medically necessary when:
医疗政策BSC_CON_2.14基因测试：癫痫，...
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