伴有家族性玻璃体混浊的原发性淀粉样变性：一个罕见病例及家族情况
Primary amyloidosis with familial vitreous opacities: an unusual case and family.
作者信息
Okayama M, Goto I, Ogata J, Omae T, Yoshida I, Inomata H
出版信息
Arch Intern Med. 1978 Jan;138(1):105-11.
PMID:202208
Abstract
Peripheral neuropathy was not found even six to ten years after the onset of visual symptoms in a family with primary amyloidosis, except in the propositus at the terminal stage. The propositus had mainly ocular and CNS involvement. An ocular manifestation, the vitreous opacity, was the only involvement in the family members, in spite of the long clinical course. This family may have a different type of familial primary amyloidosis from that previously reported.
摘要
在一个原发性淀粉样变性家族中，即使在视觉症状出现六至十年后，除了处于终末期的先证者外，未发现周围神经病变。先证者主要有眼部和中枢神经系统受累。尽管临床病程较长，但玻璃体混浊这一眼部表现是该家族成员唯一的受累情况。这个家族可能患有与先前报道不同类型的家族性原发性淀粉样变性。
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