Retinosis pigmentaria en un adolescente

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

doi:10.1016/j.bmhimx.2015.06.001

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 journal › Article › peer-review

1 Citation (Scopus)

Abstract

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 contribution	Retinitis pigmentosa in an adolescent
Original language	Spanish
Pages (from-to)	195-198
Number of pages	4
Journal	Boletin Medico del Hospital Infantil de Mexico
Volume	72
Issue number	3
DOIs	https://doi.org/10.1016/j.bmhimx.2015.06.001 https://doi.org/10.1016/j.bmhimx.2015.06.001
Publication status	Published - 2015

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Publisher Copyright:
© 2015.

All Science Journal Classification (ASJC) codes

Pediatrics, Perinatology, and Child Health

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title = "Retinosis pigmentaria en un adolescente",

abstract = "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.",

author = "{Trevi{\~n}o Alan{\'i}s}, {Mar{\'i}a Guadalupe} and {Escamilla Oca{\~n}as}, {C{\'e}sar E.} and {Gonz{\'a}lez Cerna}, Fernando and {Garc{\'i}a Flores}, {Juan B.} and {Moreno Trevi{\~n}o}, Mar{\'i}a and {Rivera Silva}, Gerardo",

note = "Publisher Copyright: {\textcopyright} 2015.",

year = "2015",

doi = "10.1016/j.bmhimx.2015.06.001",

language = "Spanish",

volume = "72",

pages = "195--198",

journal = "Boletin Medico del Hospital Infantil de Mexico",

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T1 - Retinosis pigmentaria en un adolescente

AU - Treviño Alanís, María Guadalupe

AU - Escamilla Ocañas, César E.

AU - González Cerna, Fernando

AU - García Flores, Juan B.

AU - Moreno Treviño, María

AU - Rivera Silva, Gerardo

PY - 2015

Y1 - 2015

N2 - 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.

AB - 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.

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DO - 10.1016/j.bmhimx.2015.06.001

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SN - 1665-1146

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EP - 198

JO - Boletin Medico del Hospital Infantil de Mexico

JF - Boletin Medico del Hospital Infantil de Mexico

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ER -

Retinosis pigmentaria en un adolescente

Abstract

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