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Session 4: Wednesday September 30, 2015: Anatomy of the Eye, Associated Eye Conditions and Functional Implications
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Housekeeping Questions from last week? ◦ Updates from the AES Conference in Halifax Anatomy of the Eye, Associated Eye Conditions and Functional Implications ◦ Retina
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The Retina
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Functions to convert relevant information from the external environment into a neural impulse which is sent to the brain Has two primary layers: ◦ Inner neurosensory retina ◦ Retinal pigment epithelium (RPE) When these layers separate, you get a retinal detachment
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The retina lines the posterior two thirds of the eyeball The neural retina is firmly attached anteriorly at the ora serrata (near the ciliary body) and at the margins of the optic nerve
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Posterior Pole ◦ 5-6 diameter zone situated between the superior and inferior temporal arteries
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Macula Lutea – Macula ◦ 1.5mm diameter area in the posterior pole, lateral to the optic disc
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Fovea Centralis ◦ 0.35 mm wide zone in the macula ◦ Is a depression, such that light falls directly onto the cones. ◦ Avascular
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Optic Disc ◦ 3mm medial to the centre of the macula ◦ No photoreceptors (Blind Spot)
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Peripheral Retina ◦ The remainder of the retina outside of the posterior pole ◦ Rich in rods
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RPE Photoreceptors External limiting membrane Outer nuclear layer Outer plexiform layer Inner nuclear layer Inner plexiform layer Ganglion cell layer Nerve fiber layer Internal limiting membrane Neurosensory Retina
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Pigment cell layer that nourishes the retinal cells Located just outside the retina and attached to the choroid
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2 Types ◦ Rods ◦ Cones (3 Types) Contain molecules called photopigments which absorb light ◦ Rhodopsin in the rods ◦ One in each of the three cone types Each photopigment absorbs light most effectively at different parts of the visible spectrum
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Within the photoreceptor cells, the photopigments lie in specialized membranes that are arranged in highly ordered stacks parallel to the surface of the retina Rod cells are not located in the macula, but cones are densely packed there In extreme peripheral retina there are 10 rods per cone
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RodsCones Long and narrow One visual pigment ◦ Rhodopsin No color vision 120 million in number Multiple rods connect to one nerve fiber Poor visual resolution Best in dim light (scotopic) Detect motion Short and conical Three visual pigments ◦ Chlorolabe (green light) ◦ Erythrolabe (red light) ◦ Cyanolabe (blue light) Color vision 6.5 million in number One to one cone to nerve fiber in fovea Excellent visual resolution Best in bright light (photopic)
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Is a zone that interdigitates around the rods and cones Composed of the outermost ends of Muller’s cells ◦ Muller’s cells extend vertically from the external to internal limiting membranes ◦ They lend structural and nutritional support to the retina
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Contains cell bodies of the rods and cones
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Location where rod and cone axons synapse with biploar horizontal cells
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Contains nuclei of bipolar horizontal, amacrine and Muller’s cells ◦ Transmit information within the retina
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Bipolar cells axons and ganglion cell dendrites synapse in this layer Is the location of the second and final intraocular synapse
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Contains second order neurons for vision
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Contains a roughly concentric arrangement of the one million ganglion cell axons These axons exit the eye at the optic disc and form the optic nerve
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Basement membrane which lies against the vitreous Covers the entire surface of the retina from the ora serrata up to the optic disc.
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Light entering from the left visual field … ◦ strikes the retina of the left eye on the nasal side ◦ strikes the retina of the right eye on the temporal side Light entering from the right visual field… ◦ Strikes the retina of the left eye on the temporal side ◦ Strikes the retina of the right eye on the nasal side
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Inherited disorder ◦ Affects males and females alike ◦ Autosomal recessive Affected individual has received the disease-causing gene from both parents ◦ Incidence is between 1/1660 and 1/15000 Usually diagnosed before age 20, but can start by age 6 ◦ Some may not notice significant vision loss before age 30-40 ◦ Total loss of sight is rare ◦ Vision is between 20/200-20/400
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Vision loss cannot be corrected with glasses or contact lenses ◦ No treatment is currently available It affects the macula ◦ Causes a loss of central vision ◦ Limits the person’s ability to see color and details ◦ Vision loss is caused by a loss of cone cells
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Usually diagnosed between 6-20. Can be difficult to detect. Because of the late diagnosis and often quick progress of the disease can cause emotional and acceptance issues. May have other related eye conditions.
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Low Visual Acuity (between 20/200 to 20/400) May appear to change depending on lighting. May benefit from low vision aids such as magnifiers or monoculars. May benefit from assistive technology such as CCTV, Zoomtext or Magnifier mouse. May benefit from large print. May benefit from descriptions of pictures Many of these students need to learn Braille and cane skills.
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Photophobia: When completing a FVA, test the student in different types and levels of lighting. May benefit from wearing sunglass or brimmed hat. May benefit from sitting with back to windows. Avoid objects that produce glare such as magazines or shiny toys. (Different lighting and/or positioning can reduce glare).
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Poor Contrast sensitivity: May appear to change depending on lighting. May benefit from clear and high contrasting materials i.e. black on white. May benefit from high contrasting pictures or verbal descriptions. May benefit from high contrasting marking in environment i.e. edges of stairs.
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Visual Field Loss Scotomas (blind spots) in the central visual field can cause difficulty reading and traveling. O&M, cane travel and scanning techniques are all important. A LMA may be needed if there are changes. Scotomas or Blind spots in the visual field may make reading or recognizing people and places difficult. Students with blind spots may exhibit eccentric viewing or appear to be looking to the side instead of at you. “wavy vision” or “blurry spots”
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Colour Vision: Colour vision can be affected. Label pictures that are colour dependent (i.e. maps or diagrams) with symbols or tactiles. Use high contrasting colours.
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Is an infection caused by a single-cell parasite, Toxoplasma gondii Is acquired by ◦ Contact with cats or cat feces ◦ Eating raw or undercooked meats The disease can be transmitted from mother to child during pregnancy ◦ A small percentage of these infants can be born with retinal scarring ◦ Vision loss is permanent
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Can have localized blind spots Vision can be better than 20/100 in more than half of affected individuals Reactivation of infections in old scars can cause further vision loss Treatments are available in the form of drug therapy, which can ◦ Kill the parasite ◦ Reduce inflammation ◦ Minimize scarring Treatments cannot ◦ Restore lost vision ◦ Prevent reactivation of disease
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Toxoplasmosis is a life long concern that can “pop up” late in life even though there were no initial symptoms.
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Although rare, can cause low visual acuity (20/100) May benefit from low vision aids such as magnifiers or monoculars. May benefit from assistive technology such as CCTV, Zoomtext or Magnifier mouse. May benefit from large print. May benefit from descriptions of pictures
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Retinal Scarring may cause “blind spots” Scotomas (blind spots) in the central visual field can cause difficulty reading and traveling. O&M, cane travel and scanning techniques are all important. A LMA may be needed if there are changes. Scotomas or Blind spots in the visual field may make reading or recognizing people and places difficult. Students with blind spots may exhibit eccentric viewing or appear to be looking to the side instead of at you. “wavy vision” or “blurry spots”
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Photophobia: When completing a FVA, test the student in different types and levels of lighting. May benefit from wearing sunglass or brimmed hat. May benefit from sitting with back to windows. Avoid objects that produce glare such as magazines or shiny toys. (Different lighting and/or positioning can reduce glare).
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In RP, photoreceptors are slowly damaged due to an inherited genetic mutation ◦ Many different mutations can cause RP It is slowly progressive 1/3500 Canadians has RP Early symptoms ◦ Difficulty seeing at night and in dim light conditions ◦ Loss of peripheral vision Diagnosed in childhood or early adolescence
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In RP, rod photoreceptors are lost first ◦ As more rods are lost, the cones also start to die May be triggered by rod cell death Clinical findings ◦ Mottled pattern on the retina Due to the accumulation of dark pigment ◦ Thinning of blood vessels ◦ Waxy appearance of optic nerve
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As RP progresses, peripheral vision is slowly lost Uncomfortable sensitivity to light and glare is common Eventually people with RP lose central vision, and some will go on to lose all light perception No treatment is available
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May be a part of a syndrome i.e. Ushers Syndrome, Bardet – Biedl Syndrome or Leber Congenital Amaurosis. Genetic Different forms and may look different for different people Generally causes the most problems in teenage years
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Emotional Impact and understanding. Social impact Can affect learning/ learning media.
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Visual Field Loss Constriction of peripheral fields may cause poor night vision, difficulty reading and traveling. O&M, cane travel and scanning techniques are all important. Scotomas or Blind spots in the visual field may make reading or recognizing people and places difficult. Most students with RP will begin learning Braille in preparation for vision loss.
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Photophobia: When completing a FVA, test the student in different types and levels of lighting. May benefit from wearing sunglass or brimmed hat. May benefit from sitting with back to windows. Avoid objects that produce glare such as magazines or shiny toys. (Different lighting and/or positioning can reduce glare).
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Low Visual Acuity (Depends on the progress of RP in individual person) May appear to change depending on lighting. May benefit from low vision aids such as magnifiers or monoculars. May benefit from assistive technology such as CCTV, Zoomtext or Magnifier mouse. May benefit from large print. May benefit from descriptions of pictures Most of these students need to learn Braille and cane skills.
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Colour Vision: Colour vision can be affected. Label pictures that are colour dependent (i.e. maps or diagrams) with symbols or tactiles. Use high contrasting colours.
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A rare form of eye cancer affecting the retina of infants and young children Occurs in every 1/20000 births Can be unilateral (60%) or bilateral (40%) Caused by a genetic defect in the retinoblastoma gene Presents as a white pupil
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Is treatable!!! ◦ Surgery ◦ Chemotherapy ◦ Radiation ◦ Laser Children must be re-examined regularly for the development of new tumors during the first 3 years of life ◦ Survival rate is 96% ◦ Are prone to other cancers throughout their life Visual outcome depends on the location of the tumor ◦ Close to optic nerve and macula can cause decreased acuity ◦ Toward the edge of the retina may not have an effect on vision
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If the eye is removed, it is replaced by a prosthesis to protect the orbit of the eye.
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Low Visual Acuity (Depending of placement of tumour, may cause loss of visual acuity) May benefit from low vision aids such as magnifiers or monoculars. May benefit from assistive technology such as CCTV, Zoomtext or Magnifier mouse. May benefit from large print. May benefit from descriptions of pictures
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Retinopathy of prematurity (ROP) is a potentially blinding disease caused by abnormal development of retina blood vessels in premature infants When a baby is born prematurely, the retinal blood vessels can grow abnormally When ROP is severe, it can cause the retina to pull away or detach from the wall of the eye Babies 1250 grams or less and are born before 31 weeks gestation are at highest risk
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When the eye develops, the blood vessels of the retina grow from the optic nerve toward the peripheral retina When an infant is premature, this growth is incomplete, especially at the outer edges of the retina Abnormal new blood vessels form at the edge of the developed retina ◦ This area can become scarred leading to retinal detachments Risk factors ◦ Too much/too little oxygen at birth ◦ Birth weight ◦ Genetic predisposition ◦ Blood transfusions
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Stage 1 ◦ Presence of a line between developed and undeveloped retina Stage 2 ◦ The line becomes a ridge Stage 3 ◦ New, abnormal blood vessels grow on and around the ridge Stage 4 ◦ Leakage from new vessels and scar formation result in retinal detachment Stage 5 ◦ Detachment of entire retina
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Plus Disease ◦ Rapidly worsening ROP
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Zone I ◦ Area around optic nerve and macula ◦ Poor visual outcome Zone II ◦ Area between zones I and II ◦ Intermediate prognosis Zone III ◦ Farthest edge of the retina ◦ Good prognosis
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May hear it described in “clock hours” ◦ A way of indicating how much of a zone has the disease The need for treatment is determined by ◦ Location ◦ Extent ◦ Stage of ROP Most cases do not require treatment Treatment may involve ◦ Laser (peripheral field defects) ◦ Cryotherapy (freezing retina) ◦ Treatment of retinal detachments ◦ Treament of cataracts, glaucoma
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Fewer than 20% of infants have final VA of 20/40 or better Vision problems can include ◦ Nystagmus ◦ Strabismus ◦ High myopia Require optical correction
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RoP can be diagnosed in 5 stages. The level of damage is determined by the stage. Some students will have no vision and receive Braille and Cane instruction, while others will not qualify for services. May be paired with other eye conditions.
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Low Visual Acuity (Depending on stage of RoP and the affect to the retina) May appear to change depending on lighting. May benefit from low vision aids such as magnifiers or monoculars. May benefit from assistive technology such as CCTV, Zoomtext or Magnifier mouse. May benefit from large print. May benefit from descriptions of pictures May benefit from Braille
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Photophobia: When completing a FVA, test the student in different types and levels of lighting. May benefit from wearing sunglass or brimmed hat. May benefit from sitting with back to windows. Avoid objects that produce glare such as magazines or shiny toys. (Different lighting and/or positioning can reduce glare).
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Visual Field Loss Constriction of peripheral fields may cause poor night vision, difficulty reading and traveling. O&M, cane travel and scanning techniques are all important. Scotomas or Blind spots in the visual field may make reading or recognizing people and places difficult.
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Colour Vision: Colour vision can be affected. Label pictures that are colour dependent (i.e. maps or diagrams) with symbols or tactiles. Use high contrasting colours.
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Low Contrast: May appear to change depending on lighting. May benefit from clear and high contrasting materials i.e. black on white. May benefit from high contrasting pictures or verbal descriptions. May benefit from high contrasting marking in environment i.e. edges of stairs.
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Possible poor depth perception: May benefit from high contrasting outlines on environment i.e. stairs or playground equipment. May benefit from having time to explore new areas and being warned of changes in ground level.
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Inherited disorder of pigment development Affects ◦ Eyes ◦ Skin ◦ Hair Melanin is reduced or absent ◦ Causes fair skin, blue eyes Pigment is required for the development of the retina, especially the fovea
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Two main types of Albinism (according to phenotype) ◦ Oculocutaneous Albinism Reduction or absence of melanin in the skin, hair, and optic system Pale skin appearance ◦ Ocular Albinism Changes in the optic system only with no clinical difference in skin and hair color ◦ Each category can be further divided into specific genetic mutations
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When melanin is absent: ◦ Abnormal decussation of optic nerve fibers (more next week) This leads to a predominance of monocular vision and decreased binocular depth perception. ◦ Foveal hypoplasia ◦ Congenital nystagmus Clinically can see iris transillumination
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The presentation of Albinism can be emotionally or socially difficult Commonly associated with strabismus and nystagmus. Sensitivity to the sun and light.
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Photophobia: When completing a FVA, test the student in different types and levels of lighting. May benefit from wearing sunglass or brimmed hat. May benefit from sitting with back to windows. Avoid objects that produce glare such as magazines or shiny toys. (Different lighting and/or positioning can reduce glare). Spot lighting, such as using a lamp or lighting only the necessary area may help a student with Albinism see.
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Low Visual Acuity (20/100 – 20/400) May appear to change depending on lighting. May benefit from low vision aids such as magnifiers or monoculars. May benefit from assistive technology such as CCTV, Zoomtext or Magnifier mouse. May benefit from large print. May benefit from descriptions of pictures
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Poor Contrast sensitivity: May appear to change depending on lighting. May benefit from clear and high contrasting materials i.e. black on white. May benefit from high contrasting pictures or verbal descriptions. May benefit from high contrasting marking in environment i.e. edges of stairs
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Colour Vision: Colour vision can be affected. Label pictures that are colour dependent (i.e. maps or diagrams) with symbols or tactiles. Use high contrasting colours.
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Poor depth perception (if there is strabismus): May benefit from high contrasting outlines on environment i.e. stairs or playground equipment. May benefit from having time to explore new areas and being warned of changes in ground level.
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Continue with anatomy…the visual pathway BRING COFFEE!
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