FKP Sutter, H Helbig - Survey of ophthalmology, 2003 - Elsevier Familial retinal arteriolar tortuosity is a rare disorder with autosomal
dominant inheritance. It is characterized by a pathognomic pattern of
progressive, pronounced tortuosity of the arterioles of second and third ... Cited by 14 - Related articles - All 10 versions
P Karadimas, E Hatzispasou, EA Bouzas - Journal of Neuro-Ophthalmology, 2003 - journals.lww.com Abstract: Microvascular retinal abnormalities, presenting in a corkscrew
configuration, have been very recently de- scribed in patients with
neurofibromatosis type 1 (NF-1). We report one more patient with NF-1 who ... Cited by 6 - Related articles - BL Direct - All 3 versions
NR Miller, NJ Newman - The Lancet, 2004 - Elsevier Neurological disease can involve the eye in many ways. Every structure—the
conjunctiva, cornea, anterior chamber, iris, lens, vitreous humour, retina,
choroid, and optic nerve—can be affected. In many cases, ocular ... Cited by 4 - Related articles - All 6 versions
AA Akçakaya, HH Erbil, A Olgun, A Dolar, EK … - Neuro-Ophthalmology, 2008 - informahealthcare.com Purpose: To describe the ocular angiographic findings in patients with
Neurofibromatosis type 1 (NF-1). Methods: We examined 20 consecutive patients
diagnosed with NF1 by conventional ophthalmoscopy and fluorescein ... Related articles - All 4 versions
TRVIN NEUROFIBROMATOSIS - Arch Soc Esp Oftalmol, 2005 - SciELO Espana Caso clínico: Se describe un paciente de 4 años con neurofibromatosis tipo 1
(NF-1) y vasos retinianos tortuosos de primer, segundo y tercer orden que
terminaban en forma de sacacorcho. Discusión: Los pacientes con NF-1 ... Related articles - Cached - All 2 versions
VM ASENSIO-SÁNCHEZ, B TORREBLANCA- … - oftalmo.com Las facomatosis son anomalías del desarrollo embrionario o displasias,
congénitas y hereditarias que se caracterizan por la aparición de manchas
muco-cutáneas y tumores a partir de células no diferenciadas que afecta ... Related articles - Cached