کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4029951 1262512 2007 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Oculoleptomeningeal Amyloidosis in a Patient with a TTR Val30Gly Mutation in the Transthyretin Gene
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی چشم پزشکی
پیش نمایش صفحه اول مقاله
Oculoleptomeningeal Amyloidosis in a Patient with a TTR Val30Gly Mutation in the Transthyretin Gene
چکیده انگلیسی
Amyloidosis should be considered in patients who present with vitritis that is unresponsive to corticosteroid therapy. Vitreous biopsy with histopathological analysis is recommended in these cases. Additionally, sequencing of the transthyretin gene should be considered in patients with vitreous amyloidosis to help establish known genetic syndromes and predict both ocular and systemic comorbidities. Although not described previously, elevated IOP may develop in patients with vitreous amyloidosis due to a TTR Val30Gly mutation in the transthyretin gene.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Ophthalmology - Volume 114, Issue 11, November 2007, Pages e33-e37
نویسندگان
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