Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Retinitis Pigmentosa Unilateral: Reporte de 2 Casos

View through CrossRef
Objetivo: Reportar 2 casos clínicos con diagnóstico de Retinitis Pigmentosa Unilateral. Caso Clínico: Se presentan 2 casos con Retinitis Pigmentosa unilateral. El primer caso es de una paciente femenina de 41 años con un período de seguimiento de 6 años. El segundo caso es de un paciente masculino de 69 años con catarata subcapsular asociada y un período de seguimiento de 9 años. Conclusión: La Retinitis Pigmentosa Unilateral es una presentación muy rara de la enfermedad.
Asociacion Guatemalteca de Oftalmologia
Title: Retinitis Pigmentosa Unilateral: Reporte de 2 Casos
Description:
Objetivo: Reportar 2 casos clínicos con diagnóstico de Retinitis Pigmentosa Unilateral.
Caso Clínico: Se presentan 2 casos con Retinitis Pigmentosa unilateral.
El primer caso es de una paciente femenina de 41 años con un período de seguimiento de 6 años.
El segundo caso es de un paciente masculino de 69 años con catarata subcapsular asociada y un período de seguimiento de 9 años.
Conclusión: La Retinitis Pigmentosa Unilateral es una presentación muy rara de la enfermedad.

Related Results

Retinitis Pigmentosa
Retinitis Pigmentosa
In studying the cases with typical and atypical pigmentary degeneration of the retina we strived to analyse in the clinical material all ophthalmoscopic and ocular changes together...
P.arg102ser is a common Pde6? mutation causing autosomal recessive retinitis pigmentosa in Pakistani families
P.arg102ser is a common Pde6? mutation causing autosomal recessive retinitis pigmentosa in Pakistani families
Abstract Aim: To explore the genetic cause of autosomal recessive retinitis pigmentosa in consanguineous families. Methods: The multi-centre study was conducted from Ju...
Macular abnormalities in patients with Retinitis Pigmentosa.
Macular abnormalities in patients with Retinitis Pigmentosa.
Objective: To assess the frequency of macular abnormalities identified through OCT in individuals with retinitis pigmen-tosa.Methodology: This quantitative cross-sectional research...
A Journey towards Improved Quality of Life of a Typist with Retinitis Pigmintosa
A Journey towards Improved Quality of Life of a Typist with Retinitis Pigmintosa
Abstract: Retinitis pigmentosa (RP) is a group of inherited rod-cone degenerative pathologies that present clinically with similar signs and symptoms. Common fundus findings includ...
Retinitis Pigmentosa
Retinitis Pigmentosa
Abstract Retinitis pigmentosa is a heterogeneous group of retinal dystrophies that are characterized by photoreceptor cell degeneration, night blindness, a gradual loss o...
Retinitis Pigmentosa
Retinitis Pigmentosa
Retinitis pigmentosa is a chronic, progressive, hereditary disease of unknown aetiology. The symptoms of the disease follow a set pattern of progression and usually terminate with ...
Bilateral intermediate uveitis asociated with retinosis pigmentosa
Bilateral intermediate uveitis asociated with retinosis pigmentosa
AbstractPurpose Retinitis pigmentosa (RP) is a group of inherited dystrophies with great clinical genetic and evolutionary heterogeneity. We report a patient with retinitis pigment...
Usher syndrome Type I in an adult Nepalese male: a rare case report
Usher syndrome Type I in an adult Nepalese male: a rare case report
Usher syndrome, also known as retinitis pigmentosa-dysacusis syndrome, is an extremely rare genetic disorder, characterized by retinitis pigmentosa (RP) and congenital sensorineura...

Back to Top