Retinosis pigmentaria en un adolescente

Translated title of the contribution: Retinitis pigmentosa in an adolescent

María Guadalupe Treviño Alanís, César E. Escamilla Ocañas, Fernando González Cerna, Juan B. García Flores, María Moreno Treviño, Gerardo Rivera Silva*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)


Background: Retinitis pigmentosa is the most common chronic and inherited condition of retinal dystrophy. The progressive involvement of retinal photoreceptors and other layers characterize this condition. This situation results in optic disc pallor and retinal pigment deposition vascular attenuation. Case report: We present the case of a 15-year-old male with a history of 6 months evolution characterized by night blindness and bilateral impairment of superior temporal vision. Conclusions: This type of dystrophy is a genetic and progressive eye condition that begins during adolescence and produces visual impairment.

Translated title of the contributionRetinitis pigmentosa in an adolescent
Original languageSpanish
Pages (from-to)195-198
Number of pages4
JournalBoletin Medico del Hospital Infantil de Mexico
Issue number3
Publication statusPublished - 2015

Bibliographical note

Publisher Copyright:
© 2015.

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health


Dive into the research topics of 'Retinitis pigmentosa in an adolescent'. Together they form a unique fingerprint.

Cite this