腦白質腎上腺萎縮癥
The molecular diagnosis for X-linked adrenoleukodystrophy (ALD) using mutational analysis at genomic DNA level is important. 摘要在基因組DNA水平,應用基因突變分析的方法對腎上腺腦白質營養(yǎng)不良進行分子診斷十分重要。
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). 開始(醫(yī)生)不敢診斷后來(那個醫(yī)生)請教了他在省人民醫(yī)院當教授的專家診斷的
This study aimed at understanding the expectation, planning for future and copying mechanisms of the adrenoleukodystrophy patients. 病越不會感覺到害怕,而影響他們最大的是母親與父親的態(tài)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 檢測腎上腺腦白質營養(yǎng)不良 (adrenoleukodystrophy,AL D) (MIM 3 0 0 10 0 )患者編碼AL D蛋白的 ABCD1基因 [ATP-結合盒 (ATP-binding cassette,ABC)超家族中 D亞家族 1]突變。
Adrenoleukodystrophy (ALD) is a degenerative disorder of myelin, a complex fatty neural tissue that insulates many nerves of the central and peripheral nervous systems. 什麼是'腎上腺腦白質營養(yǎng)不良-退行性疾病的神經髓鞘覆蓋'?