Casalino Giuseppe, Pierro Luisa, Manitto Maria Pia, Michaelides Michel, Bandello Francesco
San Raffaele Scientific Institute, Vita-Salute University, Milan, Italy; Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.
San Raffaele Scientific Institute, Vita-Salute University, Milan, Italy.
J AAPOS. 2018 Aug;22(4):321-323. doi: 10.1016/j.jaapos.2017.12.016. Epub 2018 Apr 12.
We report the outcome of 3 years of arginine-restricted diet and vitamin B6 supplementation in a boy who presented with gyrate atrophy of the choroid and retina and bilateral cystoid macular edema. The diagnosis of gyrate atrophy was made on the basis of clinical findings and increased plasma ornithine levels. Molecular genetic testing revealed a disease-causing homozygous mutation in the ornithine aminotransferase (OAT) gene. After 3 months of dietary modification and pyridoxine supplementation, visual acuity improved, and optical coherence tomography showed resolution of cystoid macular edema in both eyes. This anatomical and functional improvement was maintained during 3 years of follow-up.
我们报告了一名患有脉络膜和视网膜回旋状萎缩及双侧黄斑囊样水肿的男孩,接受3年精氨酸限制饮食和维生素B6补充治疗的结果。根据临床症状和血浆鸟氨酸水平升高做出了回旋状萎缩的诊断。分子基因检测显示鸟氨酸转氨酶(OAT)基因存在致病纯合突变。经过3个月的饮食调整和补充吡哆醇后,视力有所改善,光学相干断层扫描显示双眼黄斑囊样水肿消退。在3年的随访期间,这种解剖结构和功能上的改善得以维持。