Liu Yo-Tsen, Lin Kang-Hsu, Soong Bing-Wen, Liao Kwong-Kum, Lin Kon-Ping
The Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan.
Pediatr Neurol. 2007 May;36(5):348-50. doi: 10.1016/j.pediatrneurol.2006.12.009.
The ABCD1 gene mutation (previously ALD) has been reported in China, but not previously in Taiwan. This case report describes one Taiwanese patient whose clinical manifestations were compatible with adrenomyeloneuropathy. Direct sequencing for the ABCD1 gene of this patient and his mother detected a novel missense mutation, K513Q, in exon 6, the first such detected in a Taiwanese patient. Previous studies have suggested exon 6 as a possible hot segment of ABCD1 gene mutations in Chinese populations; however, most of the mutations in exon 6 presented as childhood cerebral adrenoleukodystrophy. K513Q is also the first novel mutation located within exon 6 and presenting with adult-onset adrenomyeloneuropathy in Chinese-Taiwanese.
ABCD1基因突变(以前称为ALD)在中国已有报道,但此前在台湾尚未有过报道。本病例报告描述了一名台湾患者,其临床表现与肾上腺脊髓神经病相符。对该患者及其母亲的ABCD1基因进行直接测序,在第6外显子中检测到一种新的错义突变K513Q,这是在台湾患者中首次检测到的此类突变。先前的研究表明,第6外显子可能是中国人群中ABCD1基因突变的一个热点区域;然而,第6外显子中的大多数突变表现为儿童脑型肾上腺脑白质营养不良。K513Q也是首次在台湾华裔中发现的位于第6外显子内且表现为成人型肾上腺脊髓神经病的新型突变。