Mahood J M
Postgrad Med J. 1980 Sep;56(659):658-60. doi: 10.1136/pgmj.56.659.658.
A 31-year-old woman thought to be suffering from a psychiatric illness was found to have peripheral and autonomic neuropathy, keratoconjunctivitis sicca and vitreous opacities. Her mother had died 10 years previously, aged 42 years from an undiagnosed illness with similar features. Histological proof of amyloidosis was obtained in both cases. This is the second report of familial amyloid neuropathy in an English family.
一名31岁的女性被认为患有精神疾病，却被发现患有周围神经和自主神经病变、干燥性角结膜炎以及玻璃体混浊。她的母亲在10年前去世，享年42岁，死因不明，但其病症特征与此相似。两例均获得了淀粉样变性的组织学证据。这是英国家族性淀粉样变神经病的第二例报道。
