RETINITIS PIGMENTOSA PATHOLOGICAL FINDINGS IN TWO CASES*
RETINITIS PIGMENTOSA PATHOLOGICAL FINDINGS IN TWO CASES*
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两例色素性视网膜炎的病理结果*
DOI：
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发表时间：
1956
影响因子：
4.1
通讯作者：
Wernher Group
中科院分区：
文献类型：
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作者：
Retinitis Pigmentosa;D. Lucas;Wernher Group
虽然视网膜色素变性是一种相当常见的疾病，也是导致失明的重要原因，但组织学检查的病例相对较少。Cogan(1950)在文献中发现了大约20个案例，他自己又描述了另外三个案例。这种情况最常见的表现为隐性遗传模式(Sorsby，1951)，到目前为止，所有记录家族史的病例似乎都属于这种类型。‘本文还记录了另外两个案例，其中一个案例显示了一种明确的显性遗传模式。
ALTHOUGH retinitis pigmentosa is a fairly common affection and an important cause of blindness, relatively few cases have been examined histologically. Cogan (1950) found some twenty cases in the literature and himself described three more. The condition most commonly shows a recessive mode of inheritance (Sorsby, 1951), and all the cases so far described for which family histories are recorded appear to be of this type. ' The present paper records two further cases, one of which shows a clearcut dominant mode of inheritance.