Yamamoto K, Hsu S P, Yoshida K, Ikeda S, Nakazato M, Shiomi K, Cheng S Y, Furihata K, Ueno I, Yanagisawa N
Department of Medicine (Neurology), Shinshu University School of Medicine, Matsumoto, Japan.
Muscle Nerve. 1994 Jun;17(6):637-41. doi: 10.1002/mus.880170611.
We report a family with familial amyloid polyneuropathy (FAP), showing an early-onset and a fatal outcome before age 30. Transthyretin (TTR) gene analysis showed one point mutation (T-->C change) in the second base of codon 55, and the corresponding amino acid substitution of proline (Pro) for leucine (Leu) was confirmed at the protein level. This is the first FAP family of Taiwanese origin demonstrating a causative gene abnormality, and FAP with TTR-Pro55 was considered to be more serious compared with other forms of FAP.
我们报告了一个患有家族性淀粉样多神经病(FAP)的家族,其发病早且在30岁前预后不良。转甲状腺素蛋白(TTR)基因分析显示密码子55第二个碱基处有一个点突变(T→C改变),并且在蛋白质水平证实了相应的氨基酸由亮氨酸(Leu)替换为脯氨酸(Pro)。这是首个源自台湾且证实有致病基因异常的FAP家族,与其他形式的FAP相比,TTR-Pro55型FAP被认为病情更严重。