Clinical neuroimaging biochemical and genetic features in six Chinese patients with Adrenomyeloneuropathy

摘要

BackgroundAdrenoleukodystrophy is a rare neurogenetic disease, AMN is the most common adult phenotype, such patients in China have not gotten enough attention. This article aims to study the features of AMN in Chinese patients and expand the gene spectrum of Chinese X-linked adrenoleukodystrophy (X-ALD) patients.