脑白质肾上腺萎缩症
The molecular diagnosis for X-linked adrenoleukodystrophy (ALD) using mutational analysis at genomic DNA level is important. 摘要在基因组DNA水平，应用基因突变分析的方法对肾上腺脑白质营养不良进行分子诊断十分重要。
In the city people's hospital, the doctor shot CT film for both of them. And the doctor's early diagnosis was Adrenoleukodystrophy(ALD/AMN). 开始（医生）不敢诊断后来（那个医生）请教了他在省人民医院当教授的专家诊断的
This study aimed at understanding the expectation, planning for future and copying mechanisms of the adrenoleukodystrophy patients. 病越不会感觉到害怕，而影响他们最大的是母亲与父亲的态度。
Objective To detect the mutations in exon 6 of ABCD1 gene encoding adrenoleukodystrophy protein(ALDP) in Chinese X -linked adrenoleukodystrophy (ALD,MIM 300100) patie nts. 目的 检测肾上腺脑白质营养不良 (adrenoleukodystrophy,AL D) (MIM 3 0 0 10 0 )患者编码AL D蛋白的 ABCD1基因 [ATP-结合盒 (ATP-binding cassette,ABC)超家族中 D亚家族 1]突变。
Adrenoleukodystrophy (ALD) is a degenerative disorder of myelin, a complex fatty neural tissue that insulates many nerves of the central and peripheral nervous systems. 什麽是'肾上腺脑白质营养不良-退行性疾病的神经髓鞘覆盖'?
