Bron A J, Burgess S E, Awdry P N, Oliver D, Arden G
Department of Ophthalmology, University of Oxford, UK.
Ophthalmic Paediatr Genet. 1989 Sep;10(3):185-98. doi: 10.3109/13816818909009875.
A family is described in which the father and son had chronic renal disease of early onset and bilateral optic nerve dysplasia. A further son, known to have microphthalmos died of renal disease in childhood. Optic nerve changes included coloboma in the father and Handmann's optic nerve anomaly, a condition resembling the morning glory syndrome (M.G.S.), in the son. There was electrodiagnostic and visual field evidence of optic nerve dysfunction even where acuity was relatively unaffected. The son developed central serous retinopathy, a condition frequently encountered in association with optic nerve dysplasias, including M.G.S.
本文描述了一个家族,其中父亲和儿子患有早发性慢性肾病和双侧视神经发育异常。另一个儿子已知患有小眼畸形,童年时死于肾病。视神经改变包括父亲的视盘缺损和儿子的汉德曼视神经异常,一种类似于牵牛花综合征(M.G.S.)的病症。即使视力相对未受影响,电诊断和视野检查也有视神经功能障碍的证据。这个儿子患上了中心性浆液性视网膜病变,这是一种常与包括M.G.S.在内的视神经发育异常相关的病症。