Posterior Microphthalmos Pigmentary Retinopathy Syndrome

被引:1
|
作者
Adeel, Syed Saifuddin [1 ,3 ]
Mohideen, Syed K. A. [1 ]
Sharma, Anuj [2 ]
Shah, Vinit J. [1 ]
Shetty, Adheesh [1 ]
机构
[1] Aravind Eye Hosp, Dept Retina Vitreous, Tirunelveli, Tamil Nadu, India
[2] Neoretina Eyecare Inst, Retina Serv, Hyderabad, Telangana, India
[3] Aravind Eye Hosp, Dept Retina Vitreous, SN High Rd, Tirunelveli 627001, Tamil Nadu, India
关键词
Foveoschisis; MFRP Gene; Microphthalmos; Posterior Microphthalmos; Retinitis Pigmentosa; OPTIC DISC DRUSEN; PAPILLOMACULAR FOLD; RETINITIS-PIGMENTOSA; MFRP; NANOPHTHALMOS; FOVEOSCHISIS;
D O I
10.18502/jovr.v18i2.13190
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To report a case of a rare disease entity Posterior Microphthalmos Pigmentary Retinopathy Syndrome (PMPRS) in a 47-year-old female with a brief review of literature. Case Report: A 47-year-old woman presented with a history of defective vision with an associated difficulty in night vision. Clinical workup was done, which included a thorough ocular examination showing diffuse pigmentary mottling of fundus, ocular biometry showing short axial length with normal anterior segment dimensions, electroretinography showing extinguished response, optical coherence tomography showing foveoschisis, and ultrasonography showing thickened sclera-choroidal complex. Findings were consistent with those reported by other authors with Conclusion: Posterior microphthalmia with or without other ocular and systemic associations should be suspected in cases with high hyperopia. It is mandatory to carefully examine the patient at presentation and close follow-ups are needed to maintain visual function.
引用
收藏
页码:240 / 244
页数:5
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