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Supernormal Electro-Oculograms in Patients with Neurofibromatosis Type 1

PURPOSE: To asses the retinal pigment epithelium (RPE) function measured by EOG testing in patients with neurofibromatosis type 1 (NF-1). Our preliminary EOG results suggested dysfunction of the RPE in individuals with NF-1. In order to confirm our initial results we performed EOG examination on a l...

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Detalles Bibliográficos
Autores principales: Lubiński, Wojciech, Zajączek, Stanisław, Sych, Zbigniew, Penkala, Krzysztof, Palacz, Olgierd, Lubiński, Jan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840006/
https://www.ncbi.nlm.nih.gov/pubmed/20233463
http://dx.doi.org/10.1186/1897-4287-2-4-193
Descripción
Sumario:PURPOSE: To asses the retinal pigment epithelium (RPE) function measured by EOG testing in patients with neurofibromatosis type 1 (NF-1). Our preliminary EOG results suggested dysfunction of the RPE in individuals with NF-1. In order to confirm our initial results we performed EOG examination on a larger group of NF-1 patients. PATIENTS: Studies were performed on 36 patients with clinically diagnosed NF-1 and compared to normal healthy controls. METHODS: Standard EOG recordings were performed in accordance with the International Society for Clinical Electrophysiology of Vision (ISCEV) standards. RESULTS: In NF-1 patients the Arden indexes of the EOG test were significantly higher primarily due to the lower values of dark troughs. Supernormal EOGs (exceeding the value of the mean + 2 SD from the control group) were present in 58% of NF-1 patients. CONCLUSIONS: Dysfunction of the RPE is a characteristic feature of individuals with NF-1.