Aim: To describe a distinctive spectrum of retinal microvascular abnormalities in 12 patients with neurofi-bromatosis type 1 (NF-1). Methods: This is an observational prospective study of the ocular fundus evaluated by direct ophthalmoscopy with or without fluorescein angiography, to investigate retinal microvascular abnormalities in 32 patients with NF-1 and in 30 control subjects. The evaluation included a complete general and neurological physical exam-ination and in some cases computed tomography, magnetic resonance imaging with gadolinium-DTPA, or both. Results: The occurrence of a distinctive spectrum of retinal microvascular abnormalities is described in 12 patients with NF-1 (37.5%). At the lower end of the spectrum
Purpose: Only a few reports in the literature have investigated the presence of ocular abnormalities...
Background: Neurofibromatosis Type I (NF1), also termed von Recklinghausen disease, is a rare geneti...
PurposeTo analyze ocular biometric parameters alterations of the posterior pole and choroidal abnorm...
PURPOSE: The aim of this study was to provide a classification of the different retinal vascular ar...
This study aims to describe a typical retinal microvascular abnormality in patients with neurofibrom...
Extensive retinal microvascular malformation involving both small and large retinal vessels. (Ref: B...
PURPOSE: To evaluate the prevalence, the vascular features, and the clinical diagnostic implication ...
PURPOSE: To analyze and classify neurofibromatosis type 1 (NF1) related retinal vascular abnormaliti...
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder involving aberrant ...
Copyright © 2013 Shinji Makino et al. This is an open access article distributed under the Creative ...
Neurofibromatosis Type 1 (NF1) is a rare neurocutaneous disorder transmitted in an autosomal dominan...
To evaluate the ophthalmologic features of retinal vasculature in the patients with neurofibromatosi...
To report a case of a patient with NF1 presenting with ocular findings of AV malformation, multiple ...
AbstractNeurofibromatosis type 1 (NF-1) is an autosomal dominantly inherited disease characterized b...
Purpose: To analyze ocular biometric parameters alterations of the posterior pole and choroidal abno...
Purpose: Only a few reports in the literature have investigated the presence of ocular abnormalities...
Background: Neurofibromatosis Type I (NF1), also termed von Recklinghausen disease, is a rare geneti...
PurposeTo analyze ocular biometric parameters alterations of the posterior pole and choroidal abnorm...
PURPOSE: The aim of this study was to provide a classification of the different retinal vascular ar...
This study aims to describe a typical retinal microvascular abnormality in patients with neurofibrom...
Extensive retinal microvascular malformation involving both small and large retinal vessels. (Ref: B...
PURPOSE: To evaluate the prevalence, the vascular features, and the clinical diagnostic implication ...
PURPOSE: To analyze and classify neurofibromatosis type 1 (NF1) related retinal vascular abnormaliti...
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder involving aberrant ...
Copyright © 2013 Shinji Makino et al. This is an open access article distributed under the Creative ...
Neurofibromatosis Type 1 (NF1) is a rare neurocutaneous disorder transmitted in an autosomal dominan...
To evaluate the ophthalmologic features of retinal vasculature in the patients with neurofibromatosi...
To report a case of a patient with NF1 presenting with ocular findings of AV malformation, multiple ...
AbstractNeurofibromatosis type 1 (NF-1) is an autosomal dominantly inherited disease characterized b...
Purpose: To analyze ocular biometric parameters alterations of the posterior pole and choroidal abno...
Purpose: Only a few reports in the literature have investigated the presence of ocular abnormalities...
Background: Neurofibromatosis Type I (NF1), also termed von Recklinghausen disease, is a rare geneti...
PurposeTo analyze ocular biometric parameters alterations of the posterior pole and choroidal abnorm...