報告一家族同胞4人,3例錐細胞功能不全綜合征的患兒,其中2例患兒系雙胞胎.父母體健,無眼病史,非探親聯姻,父母均否認祖輩有類似眼病.對視力障礙、眼球震顫、羞明眨眼、色覺障礙、眼底改變及遺傳等特征作了簡要討論。 (中華眼底病雜志,1993,9:55-56)
Citation: 陳世森,郞志清. 雙生子錐體細胞功能不全綜合征(附同胞三例報告). Chinese Journal of Ocular Fundus Diseases, 1993, 9(1): 55-56. doi: Copy
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