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ECTOPIA LENTIS 
AND ITS LOW VISION MANAGMENT 
Indra P Sharma 
Master of Clinical Optometry (Year I) 
Amity Medical School
Objective 
 To have a better understanding about ectopia 
lentis with regard to its pathophysiology, etiology, 
clinical manifestation and management. 
 To understand the management of ectopia lentis 
with low vision aids
Contents 
1. An overview 
2. Signs and symptoms 
3. Etiology of ectopia lentis 
4. Workup and evaluation 
5. Treatment 
6. Low Vision Management 
7. Conculsion 
8. Reference
An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference 
An Overview
Introduction 
 Ectopia lentis is defined as displacement or malposition 
of the crystalline lens of the eye. 
 1749 - Berryat first reported case of lens dislocation 
 1856- Stellwag coined the term “ectopia lentis” 
 Ectopia lentis can be : 
1. Subluxation 
2. Luxation (dislocated) 
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Subluxation 
 Condition when the 
crystalline lens is 
partially displaced but 
contained within the 
lens space. 
 Few zonular attachment 
present 
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Dislocation 
 Also known as luxated 
 When lens lies completely 
outside the lens patellar 
fossa, in the anterior 
chamber, free-floating in 
the vitreous, or directly on 
the retina. 
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Anatomy of zonules 
 The lens is suspended in its anatomic position by 
ciliary zonules (zonules of Zinn or suspensory 
ligament of Zinn) 
 Zonules fibers which run from ciliary body and 
insert into the outer layer of the lens capsule 
around the equator (1.5 mm anteriorly and 1mm 
posterior) 
 Stronger zonules in anterior capsule 
 Each zonule measures 5 to 30μm in diameter 
and is composed of bundles of microfibrils 
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Pathophysiology 
 Underlying 
pathophysiology - 
Disruption or dysfunction of 
the zonular fibers of the 
lens, regardless of cause 
(trauma or heritable 
condition) 
 The degree of zonular 
impairment determines the 
degree of lens 
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Epidemiology 
Frequency 
 A rare condition. 
 Incidence in the general population is unknown. 
Mortality/Morbidity 
 Can cause marked visual disturbance, depending the 
degree of lens displacement and the underlying etiology 
Sex 
 More common in males. 
Age 
 At any age (At birth or it may manifest late in life) 
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An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference 
Signs and Symptoms 
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Symptoms 
 Distance visual acuity (moderate to severe impairment) 
depending on position of lens 
1. Fluctuating vision dramatically as the vision may alternate 
between phakia and aphakic 
2.Progressive movement of the lens- Extreme hyperopic shift or 
myopic astigmatism 
 Poor near vision 
Due to loss of accommodative power due to weakened, 
stretched or broken zonules 
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Contd... 
 Monocular diplopia 
 Visual field defects (Due to lens induced secondary 
glaucoma) 
A 1963 histological study found that crystalline lenses that 
were 
dislocated anteriorly were associated with glaucoma 77.2% of 
the time and that crystalline lenses that were subluxed or 
dislocated 
Source: Sihota R Sood NN, Argarwal He. 1995. Traumatic glaucoma.Acta Ophthalmol Scand 
posteriorly were associated with glaucoma 87.5% of the time. 
73:252-254. 
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Contd.... 
 Painful red eye (secondary to trauma) 
 Glare and photophobia 
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An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference 
Etiology of ectopia lentis 
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Traumatic dislocation 
 Traumatic dislocation is most common cause of ectopia 
lentis. 
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Hereditary ectopia lentis without 
systemic manifestations 
Single (isolated) ectopia lentis 
 Autosomal dominant inheritance 
 Genetic defect located on chromosome 
15, causing a dysfunctional zonular 
apparatus. 
 Microspherophakia is common. 
 Present at birth, can even onset late 
 Typically, supertemporal displacement 
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Ectopia lentis et pupillae 
 Usually is bilateral and typically autosomal 
recessive. 
 characterized by asymmetric eccentric pupils 
that are displaced in the opposite direction of 
the lens dislocation (toward the most 
dysfunctional zonular fibers). 
 The irides often appear atrophic with 
transillumination defects 
 Cataracts (common) 
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Pupil may be displaced in opposite 
Single (isolated) ectopia lentis direction (ectopia lentis et pupillae) 
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Systemic conditions associated 
with ectopia lentis 
 Marfan syndrome (most frequent cause of 
hereditary ectopia lentis) 
 Homocystinuria (second most common cause of 
hereditary ectopia lentis) 
 Weil-Marchesani syndrome 
 Sulfite oxidase 
 Hyperlysinemia 
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Marfan syndrome 
 Transmitted as an autosomal dominant 
trait 
 Prevalence: approx. 5 per 100,000. 
 Mutations involving the fibrillin gene on 
chromosomes 15 and 21 and may relate 
to incompetent zonular fibers. 
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Systemic association of 
Marfan 
• Limb-trunk 
• disproportion 
• Arachnodactyly 
• Pectus excavatum 
• High-arched palate 
• Aortic dilatation, 
dissection and 
regurgitation 
• Mitral valve prolapse 
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Ocular manifestation 
 Superio-temporal 
dislocation of a lens in 80% 
of cases 
 Zonules usually intact 
 Blue sclera 
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Contd.. 
 Axial myopia  Lattice degeneration 
 Cornea plana 
 Angle anomaly and 
glaucoma 
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Homocystinuria 
 It is an inborn error of metabolism. 
 Most often caused by a deficiency of 
cystathionine b-synthetase (the enzyme 
that converts homocysteine to 
cystathionine). 
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Systemic and ocular 
manifestation 
 Malar flush and fine fair hair 
 Marfanoid habaitus 
 Increased platelet stickiness 
 Mental retardation-50% 
 Inferonasal lens 
subluxation -90% 
 Disintegretation of 
zonules Sharma IP
Weil-Marchesani Syndrome 
 Rare syndrome characterized by skeletal 
malformations 
 The inheritance pattern is not well 
understood. 
 Pupillary block glaucoma is common; 
therefore, prophylactic laser peripheral 
iridotomies are recommended. 
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Systemic and ocular 
manifestation 
 Short stature 
 Short stubby fingers 
(brachydactyly) 
 Mental handicap 
 Microspherophakia (most 
common) 
 Anterior lens subluxation 
(usually) 
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Sulfite oxidase deficiency 
 Extremely rare disorder caused by a 
defect in sulfur metabolism. 
Salient features are: 
 Progressive CNS abnormalities that 
develop within the first year of life 
 Ectopia lentis. 
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Hyperlysinemia 
 Extremely rare autosomal recessive 
enzymatic defect of amino acid 
metabolism 
Salient features: 
 Mental retardation and lens dislocation. 
 Diagnosis is made by demonstration of 
increased plasma levels of lysine. 
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Primary ocular disorders 
associated 
 Congenital glaucoma/buphthalmos 
 Pseudoexfoliation syndrome 
 Syphilis/chronic uveitis 
 Retinitis pigmentosa 
 Hypermature cataract 
 Intraocular tumor 
 High myopia 
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Systemic diseases rarely 
associated 
 Ehlers-Danlos 
syndrome 
 Crouzon disease 
 Refsum syndrome 
 Kniest syndrome 
 Mandibulofacial 
dysostosis 
 Sturge-Weber 
syndrome 
 Conradi syndrome 
 Pfaundler 
syndrome 
 Pierre Robin 
syndrome 
 Wildervanck 
syndrome 
 Sprengel deformity 
Sharma IP
An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference 
Workup and evaluation 
Sharma IP
Detailed history 
History of ocular trauma. 
History investigating possible systemic disease 
associations. 
 Cardiovascular disease in Marfan syndrome 
 Skeletal problems in Marfan syndrome,Weil-Marchesani 
syndrome or homocystinuria 
Pertinent family history 
 Consanguinity 
 Mental retardation 
 Unexplained deaths at young age 
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Ophthalmic evaluation 
Visual acuity 
 Amblyopia is a common cause of decreased 
vision in congenital ectopia lentis. 
External ocular examination 
 Orbital anatomy for hereditary malformations 
(eg, enophthalmos with facial myopathic 
appearance seen in Marfan syndrome). 
 Measure corneal diameter (megalocornea in 
Marfan syndrome). 
 Strabismus is common (secondary to amblyopia). 
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Contd.. 
Retinoscopy and and keratometry 
 Careful retinoscopy and refraction is essential, often 
revealing myopia with astigmatism. 
 Keratometry may help ascertain degree of corneal 
astigmatism. 
Slit lamp examination 
 Evaluate lens position, and identify phacodonesis or 
cataract. 
 Measure intraocular pressure. 
Dilated fundus examination 
 To rule out retinal detachment 
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Laboratory studies 
 Perform appropriate diagnostic and laboratory 
evaluation, if a hereditary condition is suspected 
 Cardiac evaluation for Marfan syndrome 
 Check serum and urine levels of homocysteine 
or methionine for homocystinuria. 
Sharma IP
Imaging studies 
A scan 
 Axial length measurement may be of benefit 
(patients with Marfan syndrome have large 
globes) 
B scan 
 For any other associated vitrous and retinal 
complications 
Sharma IP
An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference 
Treatment 
Sharma IP
Refractive management 
The key to managing lens subluxation optically is 
to 
perform two refractions: 
 1.For that portion of the pupil covered by the 
crystalline lens (myopic astigmatism zone) and 
 2. For that portion of the pupil not covered by 
the crystalline lens (highly hyperopic zone). 
Sharma IP
Contd... 
 For moderate to severe subluxation 
Option: An aphakic prescription with bifocals 
and a pharmacologic dilation 
 For lens is subluxed out of the visual axis 
(bilateral) Best option: An aphakic prescription 
 Both spectacle and contact lens may be 
helpful. 
Sharma IP
Medical management 
 If no, history of trauma, patients may 
possess a systemic disease with potentially 
deleterious effects; therefore, 
comanagement with pediatrician or internist 
is essential. 
 Dietary restriction: partially effective in 
homocystinuria. 
Sharma IP
Contd... 
 Treatment of glaucoma is dependent on the 
etiologic mechanism. 
 Pupillary block requires laser peripheral iridotomy 
or iridectomy and raised IOP treated medically. 
 Prophylactic laser iridotomy in microspherophakia. 
 Dislodged lens into the AC is initially 
pharmacological (mydriasis/cycloplegia) in 
conjunction with ocular massage through a closed 
lid. 
 Treatment of a dislocated lens in the vitreous is 
Sharma IP surgical.
Sugical treatment 
1.Nd:YAG laser zonulysis 
 to displace lens out of visual axis 
2.Lesectomy 
Lensectomy is technically challenging and are indication in the 
following: 
 Lens in the anterior chamber 
 Lens-induced uveitis 
 Lens-induced glaucoma 
 Lenticular opacity with poor visual function 
 Anisometropia or refractive error not amenable to optical 
correction (eg, in a child to prevent amblyopia) 
 Impending dislocation of the lens 
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Prevention and prognsis 
Deterrence/Prevention 
 Early diagnosis of ectopia lentis with appropriate optical 
correction can prevent amblyopia. 
Complications 
 The most common ocular complications include 
amblyopia, uveitis, glaucoma, and retinal detachment 
Prognosis 
 Depending on the degree of lens dislocation, the age of 
onset, and its associated secondary complications, most 
patients do well. 
 Trauma-associated ectopia lentis – poor visual 
prognosis 
Sharma IP
An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference 
Low vision management 
Sharma IP
Rule of thumb 
 Provide LVA to help releive the main 
symptoms first 
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Distance viewing devices 
Why do we need it? 
 To compensate for high hypermetropia or 
myopic astigmatism 
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High power lenses 
 High plus spectacle 
(aspheric lenses) 
 Aphakic contact 
lens 
(Silsoft/silsoft super plus) 
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Roving Ring Scotoma 
 Circular restriction in the peripheral VF due to 
prismatic effect of high plus lenses. 
 Aspheric lenses 
reduces this scotoma 
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Telescopes 
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Sharma IP
Near optical devices 
Why is it required? 
 To compensate for high hyperopia and loss of 
accommodation 
 Preferable near viewing devices 
1. Spectacle-mounted Reading Lenses 
2. Telemicroscopes 
3. Magnifiers 
4. Electronic Devices- CCTV 
Sharma IP
Spetacle mounted reading glasses 
Sharma IP
Telemicroscope 
 Eyeglass 
mounted 
microscopes can 
be 
made to focus at 
any 
working distance. 
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Magnifiers 
 Illuminated and non-illuminated 
 Hand held and stand magnifiers 
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Electronic magnification 
devices 
 Head mounted 
video 
display systems 
 CCTV 
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Visual field enhancing 
devices 
 Reverse telescope 
To compensate for VF 
defects due to secondary 
Glaucoma. 
 Prisms 
 Mirrors 
 Reverse Telescope 
system 
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Non-optical aids 
 Relative size and larger assistive devices 
 Glare, contrast, and lighting control 
devices 
 Handwriting and written communication 
devices 
 Medical management devices 
 Orientation and mobility management 
techniques and devices 
Sharma IP
Relative size and larger assistive 
devices 
 Large print 
 Books, magazines, newspaper, dictionaries, thesauri, 
atlas, cookbooks, encyclopedias, bibles 
 Photocopy machines ( e.g. A4 size to A3 size) 
 Computer with large prints font 
 Computer software program 
 Large print typewriters 
 Others 
 Telephone dial, bank checks, watches, clocks, calculators etc 
 Games like cross word puzzles, playing cards, chess 
checkers, bingo etc. 
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 Magic 8.0  Large print 
telephones 
Sharma IP
 Large print 
calculator 
 Playing cards 
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Glare, contrast, and lighting 
control devices 
Aphakia allows for increased transmission of UV 
radiation 
 Shades 
 Tennis shades, caps, hats, side-shields, visors 
 Filters 
 NoIR and CPF lenses 
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 Sunglasses/ photochromatic lenses to reduce 
illumination levels 
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Typoscopes – a reading guide cut 
off glare 
Glare cutter ( 390-410nm)- 
cuts 100% UVB, 99% UVA 
Sharma IP
Diplopia eliminating devices 
 Stenopeic slit 
 Aperture control contact lens 
 Pinhole lenses 
Sharma IP
Color and contrast 
adjustments 
Environmental modification Painted edges of Staircase 
Sharma IP
 Contrast in kitchen 
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Hand writing and written 
communication 
 Signature guide 
 Check guides 
 Reading guide 
 Large prints 
 Bold felt-tip pens 
 Bold line paper 
 Large print typewriters 
Sharma IP
Medical management devices 
 Monitoring blood glucose 
 Large print syringe 
 Syringe with magnifiers ( optical device) 
 Preset dosage 
 Pre-filled syringes- filled with clicking sounds 
 Monitoring blood pressure 
 Readout sphygmomanometers for hearing problems 
 Monitoring temperatures 
 Large readout thermometers and talking thermometer 
Sharma IP
 Talking colour detector 
IPS 
Sharma IP
Counselling 
 If a hereditary condition is discovered, 
appropriate genetic counseling recommended. 
 All relatives with potential risk should be 
examined. 
 Advised against playing contact sports or doing 
physically strenous activities. 
Sharma IP
An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference 
Conclusion 
Sharma IP
Take home message 
 Managing patients with ectopia lentis including 
refraction is usually difficult and needs 
expertise to manage them well. 
 As most patients with ectopia lentis are 
syndromic, co-management with other 
specialist is essential. 
 While managing patient with low vision we 
need to looks at various cause and other 
ocular association like glaucoma, retinal 
detachment and amblyopia. 
 An optometrist needs to understand the need 
of the patient and prescribe according. 
Sharma IP
An overview 
Signs and 
Symptoms 
Etiology of 
ectopia lentis 
Workup and 
evaluation 
Treatment 
Low Vision 
Management 
Conculsion 
Reference Reference 
Sharma IP
Reference 
Books 
 Jonathan A Jackson, Low Vision Mannual,2007, Butterworth 
Heineman Elsevier. 
 William J Benjamin,2006, Borish’s Clinical Refraction, 
Butterworth Heineman Elsevier. 20: 816-829 
 Lighthouse International, The Lighthouse Clinician’s Guide 
to Low Vision Practice 
 Brilliant Richard L, 1999, Essentials of Low vision Practice, 
Butterworth Heineman Elsevier. 6.8.9.10 
Websites 
 www.emedicine.medscape.com 
 www.rootatlas.com 
 en.wikipedia.org 
 www.google.com/imghp 
Sharma IP
Tashi Delek 
Sharma IP

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Ectopia lentis and its low vision management

  • 1. ECTOPIA LENTIS AND ITS LOW VISION MANAGMENT Indra P Sharma Master of Clinical Optometry (Year I) Amity Medical School
  • 2. Objective  To have a better understanding about ectopia lentis with regard to its pathophysiology, etiology, clinical manifestation and management.  To understand the management of ectopia lentis with low vision aids
  • 3. Contents 1. An overview 2. Signs and symptoms 3. Etiology of ectopia lentis 4. Workup and evaluation 5. Treatment 6. Low Vision Management 7. Conculsion 8. Reference
  • 4. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference An Overview
  • 5. Introduction  Ectopia lentis is defined as displacement or malposition of the crystalline lens of the eye.  1749 - Berryat first reported case of lens dislocation  1856- Stellwag coined the term “ectopia lentis”  Ectopia lentis can be : 1. Subluxation 2. Luxation (dislocated) Sharma IP
  • 6. Subluxation  Condition when the crystalline lens is partially displaced but contained within the lens space.  Few zonular attachment present Sharma IP
  • 7. Dislocation  Also known as luxated  When lens lies completely outside the lens patellar fossa, in the anterior chamber, free-floating in the vitreous, or directly on the retina. Sharma IP
  • 8. Anatomy of zonules  The lens is suspended in its anatomic position by ciliary zonules (zonules of Zinn or suspensory ligament of Zinn)  Zonules fibers which run from ciliary body and insert into the outer layer of the lens capsule around the equator (1.5 mm anteriorly and 1mm posterior)  Stronger zonules in anterior capsule  Each zonule measures 5 to 30μm in diameter and is composed of bundles of microfibrils Sharma IP
  • 9. Pathophysiology  Underlying pathophysiology - Disruption or dysfunction of the zonular fibers of the lens, regardless of cause (trauma or heritable condition)  The degree of zonular impairment determines the degree of lens Sharma IP
  • 10. Epidemiology Frequency  A rare condition.  Incidence in the general population is unknown. Mortality/Morbidity  Can cause marked visual disturbance, depending the degree of lens displacement and the underlying etiology Sex  More common in males. Age  At any age (At birth or it may manifest late in life) Sharma IP
  • 11. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference Signs and Symptoms Sharma IP
  • 12. Symptoms  Distance visual acuity (moderate to severe impairment) depending on position of lens 1. Fluctuating vision dramatically as the vision may alternate between phakia and aphakic 2.Progressive movement of the lens- Extreme hyperopic shift or myopic astigmatism  Poor near vision Due to loss of accommodative power due to weakened, stretched or broken zonules Sharma IP
  • 13. Contd...  Monocular diplopia  Visual field defects (Due to lens induced secondary glaucoma) A 1963 histological study found that crystalline lenses that were dislocated anteriorly were associated with glaucoma 77.2% of the time and that crystalline lenses that were subluxed or dislocated Source: Sihota R Sood NN, Argarwal He. 1995. Traumatic glaucoma.Acta Ophthalmol Scand posteriorly were associated with glaucoma 87.5% of the time. 73:252-254. Sharma IP
  • 14. Contd....  Painful red eye (secondary to trauma)  Glare and photophobia Sharma IP
  • 15. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference Etiology of ectopia lentis Sharma IP
  • 16. Traumatic dislocation  Traumatic dislocation is most common cause of ectopia lentis. Sharma IP
  • 17. Hereditary ectopia lentis without systemic manifestations Single (isolated) ectopia lentis  Autosomal dominant inheritance  Genetic defect located on chromosome 15, causing a dysfunctional zonular apparatus.  Microspherophakia is common.  Present at birth, can even onset late  Typically, supertemporal displacement Sharma IP
  • 18. Ectopia lentis et pupillae  Usually is bilateral and typically autosomal recessive.  characterized by asymmetric eccentric pupils that are displaced in the opposite direction of the lens dislocation (toward the most dysfunctional zonular fibers).  The irides often appear atrophic with transillumination defects  Cataracts (common) Sharma IP
  • 19. Pupil may be displaced in opposite Single (isolated) ectopia lentis direction (ectopia lentis et pupillae) Sharma IP
  • 20. Systemic conditions associated with ectopia lentis  Marfan syndrome (most frequent cause of hereditary ectopia lentis)  Homocystinuria (second most common cause of hereditary ectopia lentis)  Weil-Marchesani syndrome  Sulfite oxidase  Hyperlysinemia Sharma IP
  • 21. Marfan syndrome  Transmitted as an autosomal dominant trait  Prevalence: approx. 5 per 100,000.  Mutations involving the fibrillin gene on chromosomes 15 and 21 and may relate to incompetent zonular fibers. Sharma IP
  • 22. Systemic association of Marfan • Limb-trunk • disproportion • Arachnodactyly • Pectus excavatum • High-arched palate • Aortic dilatation, dissection and regurgitation • Mitral valve prolapse Sharma IP
  • 23. Ocular manifestation  Superio-temporal dislocation of a lens in 80% of cases  Zonules usually intact  Blue sclera Sharma IP
  • 24. Contd..  Axial myopia  Lattice degeneration  Cornea plana  Angle anomaly and glaucoma Sharma IP
  • 25. Homocystinuria  It is an inborn error of metabolism.  Most often caused by a deficiency of cystathionine b-synthetase (the enzyme that converts homocysteine to cystathionine). Sharma IP
  • 26. Systemic and ocular manifestation  Malar flush and fine fair hair  Marfanoid habaitus  Increased platelet stickiness  Mental retardation-50%  Inferonasal lens subluxation -90%  Disintegretation of zonules Sharma IP
  • 27. Weil-Marchesani Syndrome  Rare syndrome characterized by skeletal malformations  The inheritance pattern is not well understood.  Pupillary block glaucoma is common; therefore, prophylactic laser peripheral iridotomies are recommended. Sharma IP
  • 28. Systemic and ocular manifestation  Short stature  Short stubby fingers (brachydactyly)  Mental handicap  Microspherophakia (most common)  Anterior lens subluxation (usually) Sharma IP
  • 29. Sulfite oxidase deficiency  Extremely rare disorder caused by a defect in sulfur metabolism. Salient features are:  Progressive CNS abnormalities that develop within the first year of life  Ectopia lentis. Sharma IP
  • 30. Hyperlysinemia  Extremely rare autosomal recessive enzymatic defect of amino acid metabolism Salient features:  Mental retardation and lens dislocation.  Diagnosis is made by demonstration of increased plasma levels of lysine. Sharma IP
  • 31. Primary ocular disorders associated  Congenital glaucoma/buphthalmos  Pseudoexfoliation syndrome  Syphilis/chronic uveitis  Retinitis pigmentosa  Hypermature cataract  Intraocular tumor  High myopia Sharma IP
  • 32. Systemic diseases rarely associated  Ehlers-Danlos syndrome  Crouzon disease  Refsum syndrome  Kniest syndrome  Mandibulofacial dysostosis  Sturge-Weber syndrome  Conradi syndrome  Pfaundler syndrome  Pierre Robin syndrome  Wildervanck syndrome  Sprengel deformity Sharma IP
  • 33. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference Workup and evaluation Sharma IP
  • 34. Detailed history History of ocular trauma. History investigating possible systemic disease associations.  Cardiovascular disease in Marfan syndrome  Skeletal problems in Marfan syndrome,Weil-Marchesani syndrome or homocystinuria Pertinent family history  Consanguinity  Mental retardation  Unexplained deaths at young age Sharma IP
  • 35. Ophthalmic evaluation Visual acuity  Amblyopia is a common cause of decreased vision in congenital ectopia lentis. External ocular examination  Orbital anatomy for hereditary malformations (eg, enophthalmos with facial myopathic appearance seen in Marfan syndrome).  Measure corneal diameter (megalocornea in Marfan syndrome).  Strabismus is common (secondary to amblyopia). Sharma IP
  • 36. Contd.. Retinoscopy and and keratometry  Careful retinoscopy and refraction is essential, often revealing myopia with astigmatism.  Keratometry may help ascertain degree of corneal astigmatism. Slit lamp examination  Evaluate lens position, and identify phacodonesis or cataract.  Measure intraocular pressure. Dilated fundus examination  To rule out retinal detachment Sharma IP
  • 37. Laboratory studies  Perform appropriate diagnostic and laboratory evaluation, if a hereditary condition is suspected  Cardiac evaluation for Marfan syndrome  Check serum and urine levels of homocysteine or methionine for homocystinuria. Sharma IP
  • 38. Imaging studies A scan  Axial length measurement may be of benefit (patients with Marfan syndrome have large globes) B scan  For any other associated vitrous and retinal complications Sharma IP
  • 39. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference Treatment Sharma IP
  • 40. Refractive management The key to managing lens subluxation optically is to perform two refractions:  1.For that portion of the pupil covered by the crystalline lens (myopic astigmatism zone) and  2. For that portion of the pupil not covered by the crystalline lens (highly hyperopic zone). Sharma IP
  • 41. Contd...  For moderate to severe subluxation Option: An aphakic prescription with bifocals and a pharmacologic dilation  For lens is subluxed out of the visual axis (bilateral) Best option: An aphakic prescription  Both spectacle and contact lens may be helpful. Sharma IP
  • 42. Medical management  If no, history of trauma, patients may possess a systemic disease with potentially deleterious effects; therefore, comanagement with pediatrician or internist is essential.  Dietary restriction: partially effective in homocystinuria. Sharma IP
  • 43. Contd...  Treatment of glaucoma is dependent on the etiologic mechanism.  Pupillary block requires laser peripheral iridotomy or iridectomy and raised IOP treated medically.  Prophylactic laser iridotomy in microspherophakia.  Dislodged lens into the AC is initially pharmacological (mydriasis/cycloplegia) in conjunction with ocular massage through a closed lid.  Treatment of a dislocated lens in the vitreous is Sharma IP surgical.
  • 44. Sugical treatment 1.Nd:YAG laser zonulysis  to displace lens out of visual axis 2.Lesectomy Lensectomy is technically challenging and are indication in the following:  Lens in the anterior chamber  Lens-induced uveitis  Lens-induced glaucoma  Lenticular opacity with poor visual function  Anisometropia or refractive error not amenable to optical correction (eg, in a child to prevent amblyopia)  Impending dislocation of the lens Sharma IP
  • 45. Prevention and prognsis Deterrence/Prevention  Early diagnosis of ectopia lentis with appropriate optical correction can prevent amblyopia. Complications  The most common ocular complications include amblyopia, uveitis, glaucoma, and retinal detachment Prognosis  Depending on the degree of lens dislocation, the age of onset, and its associated secondary complications, most patients do well.  Trauma-associated ectopia lentis – poor visual prognosis Sharma IP
  • 46. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference Low vision management Sharma IP
  • 47. Rule of thumb  Provide LVA to help releive the main symptoms first Sharma IP
  • 48. Distance viewing devices Why do we need it?  To compensate for high hypermetropia or myopic astigmatism Sharma IP
  • 49. High power lenses  High plus spectacle (aspheric lenses)  Aphakic contact lens (Silsoft/silsoft super plus) Sharma IP
  • 50. Roving Ring Scotoma  Circular restriction in the peripheral VF due to prismatic effect of high plus lenses.  Aspheric lenses reduces this scotoma Sharma IP
  • 53. Near optical devices Why is it required?  To compensate for high hyperopia and loss of accommodation  Preferable near viewing devices 1. Spectacle-mounted Reading Lenses 2. Telemicroscopes 3. Magnifiers 4. Electronic Devices- CCTV Sharma IP
  • 54. Spetacle mounted reading glasses Sharma IP
  • 55. Telemicroscope  Eyeglass mounted microscopes can be made to focus at any working distance. Sharma IP
  • 56. Magnifiers  Illuminated and non-illuminated  Hand held and stand magnifiers Sharma IP
  • 57. Electronic magnification devices  Head mounted video display systems  CCTV Sharma IP
  • 58. Visual field enhancing devices  Reverse telescope To compensate for VF defects due to secondary Glaucoma.  Prisms  Mirrors  Reverse Telescope system Sharma IP
  • 59. Non-optical aids  Relative size and larger assistive devices  Glare, contrast, and lighting control devices  Handwriting and written communication devices  Medical management devices  Orientation and mobility management techniques and devices Sharma IP
  • 60. Relative size and larger assistive devices  Large print  Books, magazines, newspaper, dictionaries, thesauri, atlas, cookbooks, encyclopedias, bibles  Photocopy machines ( e.g. A4 size to A3 size)  Computer with large prints font  Computer software program  Large print typewriters  Others  Telephone dial, bank checks, watches, clocks, calculators etc  Games like cross word puzzles, playing cards, chess checkers, bingo etc. Sharma IP
  • 61.  Magic 8.0  Large print telephones Sharma IP
  • 62.  Large print calculator  Playing cards Sharma IP
  • 63. Glare, contrast, and lighting control devices Aphakia allows for increased transmission of UV radiation  Shades  Tennis shades, caps, hats, side-shields, visors  Filters  NoIR and CPF lenses Sharma IP
  • 64.  Sunglasses/ photochromatic lenses to reduce illumination levels Sharma IP
  • 65. Typoscopes – a reading guide cut off glare Glare cutter ( 390-410nm)- cuts 100% UVB, 99% UVA Sharma IP
  • 66. Diplopia eliminating devices  Stenopeic slit  Aperture control contact lens  Pinhole lenses Sharma IP
  • 67. Color and contrast adjustments Environmental modification Painted edges of Staircase Sharma IP
  • 68.  Contrast in kitchen Sharma IP
  • 69. Hand writing and written communication  Signature guide  Check guides  Reading guide  Large prints  Bold felt-tip pens  Bold line paper  Large print typewriters Sharma IP
  • 70. Medical management devices  Monitoring blood glucose  Large print syringe  Syringe with magnifiers ( optical device)  Preset dosage  Pre-filled syringes- filled with clicking sounds  Monitoring blood pressure  Readout sphygmomanometers for hearing problems  Monitoring temperatures  Large readout thermometers and talking thermometer Sharma IP
  • 71.  Talking colour detector IPS Sharma IP
  • 72. Counselling  If a hereditary condition is discovered, appropriate genetic counseling recommended.  All relatives with potential risk should be examined.  Advised against playing contact sports or doing physically strenous activities. Sharma IP
  • 73. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference Conclusion Sharma IP
  • 74. Take home message  Managing patients with ectopia lentis including refraction is usually difficult and needs expertise to manage them well.  As most patients with ectopia lentis are syndromic, co-management with other specialist is essential.  While managing patient with low vision we need to looks at various cause and other ocular association like glaucoma, retinal detachment and amblyopia.  An optometrist needs to understand the need of the patient and prescribe according. Sharma IP
  • 75. An overview Signs and Symptoms Etiology of ectopia lentis Workup and evaluation Treatment Low Vision Management Conculsion Reference Reference Sharma IP
  • 76. Reference Books  Jonathan A Jackson, Low Vision Mannual,2007, Butterworth Heineman Elsevier.  William J Benjamin,2006, Borish’s Clinical Refraction, Butterworth Heineman Elsevier. 20: 816-829  Lighthouse International, The Lighthouse Clinician’s Guide to Low Vision Practice  Brilliant Richard L, 1999, Essentials of Low vision Practice, Butterworth Heineman Elsevier. 6.8.9.10 Websites  www.emedicine.medscape.com  www.rootatlas.com  en.wikipedia.org  www.google.com/imghp Sharma IP

Editor's Notes

  1. Frequency Ectopia lentis is a rare condition. Incidence in the general population is unknown. The most common cause of ectopia lentis is trauma. Mortality/Morbidity Ectopia lentis may cause marked visual disturbance, depending the degree of lens displacement and the underlying etiologic abnormality. Sex Males appear more prone to ocular trauma than females; therefore, a male preponderance has been reported. Male and female frequency varies with the etiology of the lens displacement. Age Ectopia lentis can occur at any age. It may be present at birth, or it may manifest late in life.