Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

PURPOSE To describe the clinical and molecular characteristics of patients with childhood-onset Stargardt disease (STGD). DESIGN Retrospective case series. PARTICIPANTS Forty-two patients who were diagnosed with STGD in childhood at a single institution between January 2001 and January 2012. METHODS A detailed history and a comprehensive ophthalmic examination were undertaken, including c...

متن کامل

Fine central macular dots associated with childhood-onset Stargardt Disease.

Booij JC, Baas DC, Beisekeeva J, Gorgels TG & Bergen AA (2010): The dynamic nature of Bruch’s membrane. Prog Retin Eye Res 29: 1–18. Finger RP, Charbel Issa P, Schmitz-Valckenberg S, Holz FG & Scholl HN (2011): Longterm effectiveness of intravitreal bevacizumab for choroidal neovascularization secondary to angioid streaks in pseudoxanthoma elasticum. Retina 31: 1268–1278. Gliem M, De Zeaytijd J...

متن کامل

Progression of Late-Onset Stargardt Disease.

Purpose Identification of sensitive biomarkers is essential to determine potential effects of emerging therapeutic trials for Stargardt disease. This study aimed to describe the natural history of late-onset Stargardt, and demonstrates the accuracy of retinal pigment epithelium (RPE) atrophy progression as an outcome measure. Methods We performed a retrospective cohort study collecting multic...

متن کامل

Definition of phenotypic characteristics of childhood-onset inflammatory bowel disease.

BACKGROUND & AIMS Childhood-onset inflammatory bowel disease (IBD) might be etiologically different from adult-onset IBD. We analyzed disease phenotypes and progression of childhood-onset disease and compared them with characteristics of adult-onset disease in patients in Scotland. METHODS Anatomic locations and behaviors were assessed in 416 patients with childhood-onset (276 Crohn's disease...

متن کامل

Leber’s hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients

BACKGROUND Leber's hereditary optic neuropathy (LHON) is a mitochondrial disease that typically causes bilateral blindness in young men. Here we describe the clinical and molecular characteristics of 20 patients with disease onset after the age of 50 years (late onset-LHON). METHODS From a cohort of 251 affected and 277 unaffected LHON carriers, we identified 20 patients with onset of visual ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Ophthalmology

سال: 2015

ISSN: 0161-6420

DOI: 10.1016/j.ophtha.2014.08.012