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• Retinitis_pigmentosa abstract "Retinitis pigmentosa (RP) is an inherited, degenerative eye disease that causes severe vision impairment and often blindness. The progress of RP is not consistent. Some people will exhibit symptoms from infancy, others may not notice symptoms until later in life. Generally, the later the onset, the more rapid is the deterioration in sight.[citation needed] Those who do not have RP have 90 degree peripheral vision, while some people who have RP have less than 90 degrees.A form of retinal dystrophy, RP is caused by abnormalities of the photoreceptors (rods and cones) or the retinal pigment epithelium (RPE) of the retina leading to progressive sight loss. Affected individuals may experience defective light to dark, dark to light adaptation or nyctalopia (night blindness), as the result of the degeneration of the peripheral visual field (known as tunnel vision). Sometimes, central vision is lost first causing the person to look sidelong at objects.The effect of RP is best illustrated by comparison to a television or computer screen. The pixels of light that form the image on the screen equate to the millions of light receptors on the retina of the eye. The fewer pixels on a screen, the less distinct will be the images it will display. Fewer than 10 percent of the light receptors in the eye receive the colored, high intensity light seen in bright light or daylight conditions. These receptors are located in the center of the circular retina. The remaining 90 percent of light receptors receive gray-scale, low intensity light used for low light and night vision and are located around the periphery of the retina. RP destroys light receptors from the outside inward, from the center outward, or in sporadic patches with a corresponding reduction in the efficiency of the eye to detect light. This degeneration is progressive and has no known cure.".
• Retinitis_pigmentosa icd10 "H35.5".
• Retinitis_pigmentosa icd9 "362.74".
• Retinitis_pigmentosa medlineplus "001029".
• Retinitis_pigmentosa meshId "D012174".
• Retinitis_pigmentosa omim "268000".
• Retinitis_pigmentosa thumbnail Fundus_of_patient_with_retinitis_pigmentosa,_mid_stage.jpg?width=300.
• Retinitis_pigmentosa wikiPageExternalLink how-does-argus-ii-produce-sight.
• Retinitis_pigmentosa wikiPageExternalLink 1227488-diagnosis.
• Retinitis_pigmentosa wikiPageExternalLink C2ORF71cure.
• Retinitis_pigmentosa wikiPageExternalLink ucm339824.htm.
• Retinitis_pigmentosa wikiPageExternalLink NBK1417.
• Retinitis_pigmentosa wikiPageID "350926".
• Retinitis_pigmentosa wikiPageRevisionID "604939134".
• Retinitis_pigmentosa caption "Fundus of patient with retinitis pigmentosa, mid stage From a review by Christian Hamel, 2006.".
• Retinitis_pigmentosa genereviewsname "Retinitis Pigmentosa Overview".
• Retinitis_pigmentosa genereviewsnbk "NBK1417".
• Retinitis_pigmentosa hasPhotoCollection Retinitis_pigmentosa.
• Retinitis_pigmentosa icd "362.74".
• Retinitis_pigmentosa icd "H35.5".
• Retinitis_pigmentosa medlineplus "1029".
• Retinitis_pigmentosa meshid "D012174".
• Retinitis_pigmentosa name "Retinitis Pigmentosa".
• Retinitis_pigmentosa omim "268000".
• Retinitis_pigmentosa wordnet_type synset-disease-noun-1.
• Retinitis_pigmentosa subject Category:Blindness.
• Retinitis_pigmentosa subject Category:Channelopathy.
• Retinitis_pigmentosa subject Category:Disorders_of_choroid_and_retina.
• Retinitis_pigmentosa type Abstraction100002137.
• Retinitis_pigmentosa type Attribute100024264.
• Retinitis_pigmentosa type Condition113920835.
• Retinitis_pigmentosa type Disease114070360.
• Retinitis_pigmentosa type Disorder114052403.
• Retinitis_pigmentosa type DisordersOfChoroidAndRetina.
• Retinitis_pigmentosa type IllHealth114052046.
• Retinitis_pigmentosa type Illness114061805.
• Retinitis_pigmentosa type PathologicalState114051917.
• Retinitis_pigmentosa type PhysicalCondition114034177.
• Retinitis_pigmentosa type State100024720.
• Retinitis_pigmentosa type Disease.
• Retinitis_pigmentosa type AilmentCondition.
• Retinitis_pigmentosa type Situation.
• Retinitis_pigmentosa comment "Retinitis pigmentosa (RP) is an inherited, degenerative eye disease that causes severe vision impairment and often blindness. The progress of RP is not consistent. Some people will exhibit symptoms from infancy, others may not notice symptoms until later in life.".
• Retinitis_pigmentosa label "Retinite pigmentosa".
• Retinitis_pigmentosa label "Retinite pigmentosa".
• Retinitis_pigmentosa label "Retinitis pigmentosa".
• Retinitis_pigmentosa label "Retinitis pigmentosa".
• Retinitis_pigmentosa label "Retinopathia pigmentosa".
• Retinitis_pigmentosa label "Retinopatia barwnikowa".
• Retinitis_pigmentosa label "Retinosis pigmentaria".
• Retinitis_pigmentosa label "Rétinite pigmentaire".
• Retinitis_pigmentosa label "التهاب الشبكية الصباغي".
• Retinitis_pigmentosa label "網膜色素変性症".
• Retinitis_pigmentosa label "視網膜色素變性".
• Retinitis_pigmentosa sameAs Retinopathia_pigmentosa.
• Retinitis_pigmentosa sameAs Retinosis_pigmentaria.
• Retinitis_pigmentosa sameAs Rétinite_pigmentaire.
• Retinitis_pigmentosa sameAs Retinite_pigmentosa.
• Retinitis_pigmentosa sameAs 網膜色素変性症.
• Retinitis_pigmentosa sameAs 망막색소변성증.
• Retinitis_pigmentosa sameAs Retinitis_pigmentosa.
• Retinitis_pigmentosa sameAs Retinopatia_barwnikowa.
• Retinitis_pigmentosa sameAs Retinite_pigmentosa.
• Retinitis_pigmentosa sameAs m.01z86m.
• Retinitis_pigmentosa sameAs Q847057.
• Retinitis_pigmentosa sameAs Q847057.
• Retinitis_pigmentosa sameAs 992.
• Retinitis_pigmentosa sameAs C0035334.
• Retinitis_pigmentosa sameAs Retinitis_pigmentosa.
• Retinitis_pigmentosa wasDerivedFrom Retinitis_pigmentosa?oldid=604939134.
• Retinitis_pigmentosa depiction Fundus_of_patient_with_retinitis_pigmentosa,_mid_stage.jpg.
• Retinitis_pigmentosa isPrimaryTopicOf Retinitis_pigmentosa.
• Retinitis_pigmentosa name "Retinitis Pigmentosa".