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摘要


本篇報告一個由於水晶體移位引起續發性青光眼之一例,並做其家族史追踪,發現其父親和妹妹均有水晶體移位的現象,因此針對此點做分析和探討。

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並列摘要


A case of secondary Glaucoma induced by Lens dislocation is reported. Family history with dominant inheritance is also noticed. After a serial differential diagnosis, the final diagnosis is ”Dominant Microspherophakia”. Dominant Microspherophakia is a disease entirely characterized by: 1. Small Lens, spherophakia. 2. An isolated anomaly. 3. Lens dislocation. 4. Autosomal dominant inheritance. 5. Spherophakia may be due to dominant mutation from father or mother.

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