- 期刊
- OpenAccess
Alport氏徵候羣－病例報告
Alport's Syndrome-A Case Report
摘要
本篇報告一病例其主要症狀為視力模糊，聽力喪失及長久以來的兩側腰痛，臨床檢查發現眼部有前圓錐狀水晶體及輕度晶體囊下白內障，聽力記錄圖呈感覺性聽力衰退曲線，腎臟則有功能受損及重度血尿、蛋白尿情形，其特徵完全符合Alport氏症候群的診斷要件。
關鍵字
無資料並列摘要
Alport's syndrome is a hereditary disease characterized by progressive hemorrhagic nephritis and sensorineural hearing loss. The association of ocular abnormalities with Alport's syndrome was first reported by Sohar in 1956; and since then they have been seen in approximately 14% of cases. We report a young male of Alport's syndrome with progressive nephritis, sensorineural hearing loss and the most commomly associated ocular abnormalities-lenticonus and subcapsular cataract. Though his family history provides no definite evidence of the same syndrome in other members, we believe he is a case of Alport's syndrome because of his classic signs. Since Alport's syndrome affects male patient much more severely than female, with affected males dying of uremia in the second or third decade of life, we'll keep on following up this case.
延伸閱讀
- 古春瑜、陳清煌（1989）。Alport氏症候群－病例報告。中華民國眼科醫學會雜誌，28(2)，493-496。https://doi.org/10.30048/ACTASOS.198905.0090
- 吳志修、楊怡和（1993）。Lermoyez氏症候群－病例報告。中華民國耳鼻喉科醫學會雜誌，28(6)，395-398。https://doi.org/10.6286/1993.28.6.395
- 梁德城、饒宇東、李慶雲（1975）。Reye氏症候羣：一病例報告。Acta Paediatrica Sinica，16(1)，22-25。https://www.airitilibrary.com/Article/Detail?DocID=00016578-197503-16-1-22-25-a
- 顏宗弦、胡克信（1997）。Kartagener氏症候群－病例報告。中華民國耳鼻喉科醫學會雜誌，32(5)，450-454。https://doi.org/10.6286/1997.32.5.450
- 陳建焜、林清淵（1992）。Alport's Syndrome。Acta Paediatrica Sinica，33(s_1)，19-21。https://www.airitilibrary.com/Article/Detail?DocID=00016578-199201-33-s_1-19-21-a