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Congenital Anomalies in ChildrenANDREA LEUNG, MD FRCSC
OCTOBER 31, 2015
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Objectives1. To outline common pediatric congenital anomalies involving ocular alignment, motility, the
anterior segment and the posterior segment
2. To review the important steps in diagnosing, treating and managing pediatric ocular congenital anomalies
3. To discuss red flags and vision or life-threatening features of various pediatric congenital anomalies
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Anterior Segment Anomalies
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Pediatric Lens Disorders•Abnormalities:
◦ Opacification (Lamellar, nuclear, lenticonus/ lentiglobus, polar, posterior subcapsular)◦ Size (Microspherophakia)◦ Shape (Spherophakia, coloboma)◦ Location (Subluxed)◦ Development (Persistent fetal vasculature/ PHPV)
• Congenital cataracts – 1:250 incidence• Usually >3mm = visually significant
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Congenital Cataracts(Pictures)
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Unilateral Congenital Cataract - Etiology• Ocular anomalieso Colobomao Aniridiao Uveitiso Anterior segment dysgenesiso Posterior segment tumours
• Idiopathic
• Trauma – R/O non-accidental injury
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Non-Accidental Injury**ALWAYS BE ALERT TO POSSIBLE NON-ACCIDENTAL INJURY**
• A dilated exam is criticaloWhite centered hemorrhagesoMacular schesiso Vitrous hemorrhageo Disc edema
• Other findings include:o Altered level of consciousnesso Bruises o Long bone / spiral fracturesoMultiple injuries in various stages of healing
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Bilateral Congenital Cataracts - Etiology◦ Craniofacial
◦ Hallerman-Streiff, Rubenstein-Taybi, Smith-Lemli-Opitz, Other
◦ Hereditary (autosomal dominant)◦ Idiopathic◦ Metabolic
◦ Galactosemia, Fabry, Wilson, mannisidosis, diabetes
◦ Infection (TORCH)◦ Toxoplasmosis, Syphilis, Rubella, CMV, Varicella
◦ Poison (Toxic)◦ Corticosteroids, radiation
◦ Chromosomal abnormality◦ Trisomy 21 (Down), 18 (Edward), 13 (Patau),
Other
◦ Renal◦ Lowe, Alport
◦ Muscloskeletal◦ Conradi, Albright, myotonic dystrophy
◦ Ocular abnormalities◦ Aniridia, anterior segment dysgenesis
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Congenital Cataract Assessment - HistoryHistory:
- Pregnancy: infections?
- Medical history: growth and development
- Family history: cataracts
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Congenital Cataract Assessment - Exam• Examine family members• Visual Function
◦ < 2 mos – fixation reflex not developed (absence is not abnormal)◦ >3mos preverbal – look at fixation behaviour, preference, objection to occlusion◦ School age – aim for 20/50 or better for school, driving◦ Bilateral – look at behaviour◦ Unilateral – surgery if VA <20/50-70 with optical and amblyopia treatment
• Visually significant ◦ Anterior capsular opacities occluding entire pupil (no RR)◦ Post/ Central opacities - >3mm diam◦ Late: (indicates optimal time for treatment past, but can still improve)
◦ Strabismus – unilateral cat◦ Nystagmus – bilateral cat
◦ Can observe patients who have significant RR around opacity OR have an opacity with clear areas within
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Congenital Cataract - WorkupUnilateral – no lab workup
Bilateral◦ No investigations needed if +FHx OR parents have congenital lens opacities◦ Labs:
◦ TORCH titer◦ VDRL◦ Urine for reducing substances, amino acids◦ Serum PO4-◦ Serum Ca2+◦ Red cell galactokinase level◦ Serum ferritin
◦ Consults◦ Genetics◦ Metabolics◦ Developmental peds
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Congenital Cataract - Treatment** NOT ALL CATARACTS NEED SURGERY!! **
• Good cycloplegic and subjective refraction
• Amblyopia management with glasses +/- patching
• Phenylephrine prior to patching in unilateral cases
• Importance of follow up for vision monitoring
• Lensectomy surgery when appropriate
• Secondary intraocular lens (depends on age, history of uveitis, cause of cataract)
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Pediatric Lens Disorders• Long discussion with parents are critical
• Prognosis• Surgery & postoperative course • Risks (aphakic glaucoma)• Visual rehabilitation (glasses, patching)• Realistic expectations• Systemic conditions
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Ectopia Lentis• Subluxation of the lens
• May be very subtle and only detectable on slit lamp examination when fully dilated • Children may present with progressive myopia and increasing astigmatism
• History: o Family history of connective tissue diseases, Marfan Syndromeo Medical history: developmental delay?o Ocular history: trauma?
• Examination:o Visual acuityo Slit lamp exam – Phacodonesis? Iridodonesis? Stretched or broken zonules?o Cycloplegic refraction
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Ectopia Lentis - Etiology- trauma
- Marfan Syndrome
- Homocystinuria
- Sulfite Oxidase Deficiency
(pictures)
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Systemic Associations with Ectopia Lentis(pictures)
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Management of Ectopia Lentis• Amblyopia management
• Correct refractive correction
• Look at position of lens• Bisecting pupil or extremely high astigmatism causing amblyopia = surgical lensectomy• Completely subluxed lens in vitreous or out of visual axis = treat as an aphakic patient (no lensectomy)
• Secondary sutured or iris-claw lenses are possible after lensectomy
• Pediatrician or pediatric geneticist to manage systemic investigations (if required)
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Posterior Segment Anomalies
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Colobomas• A coloboma is a malformation that occurs in utero when one part of the eye fails to form due to improper fusion of the optic fissure
• Colobomas can occur in isolation or with other genetic syndromes
• Colobomas can affecto Eyelido LensoMaculao Optic nerveo Uvea
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Colobomas(pictures)o Eyelido LensoMaculao Optic nerveo Uvea
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Systemic Conditions Associated with Colobomas(pictures)
CHARGE, etc
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Management of Choroidal Colobomas• Referral to pediatrician or pediatric geneticist
• Long discussion with family regarding guarded visual prognosis
• Management of other associated ocular conditions • Cataracts• Microphthalmia• Increased risk of detached retina - retina is hypoplastic overlying chroidal colobomas
• Amblyopia management
• Refractive correction if needed
• Watch for development of sensory strabismus and nystagmus
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Optic Disc Drusen• Most common form of pseudopapilledema
• Other causes: hyperopia, mylinated NFL, hyaloid traction on disc
•Etiology: Cause is axonal degeneration
• Elevated optic nerve on examination +/- blurred disc margins, isolated hemorrhage, VF defect• Possible grey or yellow-white disc discolouration
• Superficial drusen may create “lumpy” yellow disc elevation, “grape-like” clusters
• Bilateral in 2/3 of patients, buried drusen in 86%• Becomes more obvious with age (mean age at diagnosis 12.1 years)
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Optic Disc Drusen(pictures)
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Papilledema• Red flags on history:o Headaches, nausea, vomiting o “Whooshing” sound in earso Worsening headache noted after change in position (bending down)o Neurologic symptomso Lethargy, loss of consciousness
•Red Flags on Examination:o Decreased visiono Visual field defecto Blurred disc margins, disc hemorrhageso (Absent spontaneous venous pulsations – absent in 25% of normal)
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Optic Disc Drusen• Investigations:o B-Scan / CT scano HVF 24-2 / Goldmann VF – may show arcuate defecto Possible MRI brain and neurology referral if increased ICP is suspected
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Motility Disorders
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Duane Retraction Syndrome• Congenital absence of 6th cranial nerve nucleus, lateral rectus is supplied by 3rd nerve
• Type I: Abduction defect
• Type II: Adduction defect
• Type III: Abduction and Adduction defect
• Features:o Ocular alignment (orthophoric, esotropic or exotropic)o Face turn possibleo Upshoot or downshoot of eye in adductiono Narrowing of palpebral fissure with adduction
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Systemic Associations with Duane Syndrome• Etiology: (pictures)o Isolatedo Goldenhaar Syndromeo Klippel-Feil Syndrome
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Duane Syndrome• Has tendency to affect left eye > right eye
• Affects girls > boys
• Goal: Maintain binocular single vision in primary position
• Surgical intervention offered when:o Significant anomalous head positiono Overshoot or undershooto Esotropia or exotropia in primary gaze
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Möbius Syndrome• Congenital developmental disorder affecting brainstem o 6th and 7th nerve palsies (lack of facial expressions, unilateral or bilateral abduction defects)o Feeding difficulties
o Oral: Micrognathia, high arched palate, cleft palate, missing/ misaligned teetho Hypotonia, digit anomalies o Hearing losso Possible developmental delay (gross motor)
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Möbius Syndrome• Congenital developmental disorder affecting brainstem o 6th and 7th nerve palsies (lack of facial expressions, unilateral or bilateral abduction defects)o Feeding difficulties
o Oral: Micrognathia, high arched palate, cleft palate, missing/ misaligned teetho Hypotonia, digit anomalies o Hearing losso Possible developmental delay (gross motor)
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Mobius Syndromepictures
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Objectives1. To outline common pediatric congenital anomalies involving ocular motility, the anterior
segment and the posterior segment
2. To review the important steps in diagnosing, treating and managing pediatric ocular congenital anomalies
3. To discuss red flags and vision or life-threatening features of various pediatric congenital anomalies
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Overview• Anterior Segment Anomalies
• Pediatric Cataracts• Ectopia Lentis
• Posterior Segment Anomalieso Choroidal colobomao Optic disc drusen
• Motility Disorderso Duane Retraction SyndromeoMöbius Syndrome
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ReferencesHoyt
AAPOS