کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6201118 1262419 2014 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Natural History and Retinal Structure in Patients with Usher Syndrome Type 1 Owing to MYO7A Mutation
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی چشم پزشکی
پیش نمایش صفحه اول مقاله
Natural History and Retinal Structure in Patients with Usher Syndrome Type 1 Owing to MYO7A Mutation
چکیده انگلیسی
MYO7A-related ocular disease is variable. Central vision typically remains preserved at least until the third decade of life, with 50% of affected individuals reaching legal blindness by 40 years of age. Distinct phenotypic subsets were identified on FAF imaging. A specific allele, previously reported in nonsyndromic deafness, may be associated with a mild retinopathy.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Ophthalmology - Volume 121, Issue 2, February 2014, Pages 580-587
نویسندگان
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