PubMed ID: 21975531Purpose: Neurofibromatosis 1 (NF1) is an autosomal dominant, multisystem disorder that also effects the eye. Herein, we aimed to investigate the posterior iris surface and ciliary body morphology of NF1 patients by ultrasonic biomicroscopy (UB). Materials & Methods: Nine consecutive unrelated subjects with NF1, and as a control group 25 healthy subjects, were included in the study. All patients underwent ophthalmic examination including visual acuity testing, slit-lamp biomicroscopy, tonometry, gonioscopy (Schaffer classification), and dilated ophthalmoscopy, UB. Results: Mean age was 35.1±16.2 (range, 11-57) and 34.5±15.6 (range, 9-60) for NF1 and control groups respectively (p<0.05). Lisch nodules were present in 16 of ...
PURPOSE: The aim of this study was to provide a classification of the different retinal vascular ar...
Aim: To investigate the incidence and clinical features of primary iris and ciliary body cysts in Ch...
Objective: Neurofibromatosis type 2 (NF2) is an uncommon but well-recognized disorder characterized ...
Purpose: We investigated the molecular causes of an unusual pigmented and ulcerated iris lesion det...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder with an autosomal dominant transmission an...
Purpose: To analyze biometric changes and prevalence of refractive in patients with neurofibromatosi...
Purpose: To analyze ocular biometric parameters alterations of the posterior pole and choroidal abno...
Objective: To describe plateau iris syndrome associated with multiple neuroepithelial cysts of the p...
Purpose: Only a few reports in the literature have investigated the presence of ocular abnormalities...
BACKGROUND: Neurofibromatosis type 1 (NF-1) is an autsomal dominant disorder which can occasionally...
Background: Neurofibromatosis Type I (NF1), also termed von Recklinghausen disease, is a rare geneti...
Lisch nodules are the most common type of ocular involvement in NF-1. Lisch nodules are melanocytic ...
Neurofibromatosis (NF) is an inherited disease affecting multiple systems in the body. The eye is fr...
INTRODUCTION: The object of this study is to understand abnormal dynamic of cerebrospinal fluid (CSF...
Purpose: The aim of this study is to evaluate ocular surface morphological and functional changes in...
PURPOSE: The aim of this study was to provide a classification of the different retinal vascular ar...
Aim: To investigate the incidence and clinical features of primary iris and ciliary body cysts in Ch...
Objective: Neurofibromatosis type 2 (NF2) is an uncommon but well-recognized disorder characterized ...
Purpose: We investigated the molecular causes of an unusual pigmented and ulcerated iris lesion det...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder with an autosomal dominant transmission an...
Purpose: To analyze biometric changes and prevalence of refractive in patients with neurofibromatosi...
Purpose: To analyze ocular biometric parameters alterations of the posterior pole and choroidal abno...
Objective: To describe plateau iris syndrome associated with multiple neuroepithelial cysts of the p...
Purpose: Only a few reports in the literature have investigated the presence of ocular abnormalities...
BACKGROUND: Neurofibromatosis type 1 (NF-1) is an autsomal dominant disorder which can occasionally...
Background: Neurofibromatosis Type I (NF1), also termed von Recklinghausen disease, is a rare geneti...
Lisch nodules are the most common type of ocular involvement in NF-1. Lisch nodules are melanocytic ...
Neurofibromatosis (NF) is an inherited disease affecting multiple systems in the body. The eye is fr...
INTRODUCTION: The object of this study is to understand abnormal dynamic of cerebrospinal fluid (CSF...
Purpose: The aim of this study is to evaluate ocular surface morphological and functional changes in...
PURPOSE: The aim of this study was to provide a classification of the different retinal vascular ar...
Aim: To investigate the incidence and clinical features of primary iris and ciliary body cysts in Ch...
Objective: Neurofibromatosis type 2 (NF2) is an uncommon but well-recognized disorder characterized ...