TY - JOUR AU - Zhang, Kaiyan AU - Sun, Xuyang AU - Chen, Yingying AU - Zhong, Qionglei AU - Lin, Lin AU - Gao, Yuan AU - Hong, Fanlin PY - 2018 DA - 2018/12/12 TI - Doyne honeycomb retinal dystrophy/malattia leventinese induced by EFEMP1 mutation in a Chinese family JO - BMC Ophthalmology SP - 318 VL - 18 IS - 1 AB - Doyne honeycomb retinal dystrophy (DHRD)/malattia leventinese (ML) is a rare allelic condition with massive drusen in the posterior fundus caused by EFEMP1 gene mutation. Patients showed decreased vision when the lesion affected the macular area. At present, the treatment efficiency is not satisfactory. SN - 1471-2415 UR - https://doi.org/10.1186/s12886-018-0988-7 DO - 10.1186/s12886-018-0988-7 ID - Zhang2018 ER -