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by Wadih Zein, MD
Cataract
Trisomy 13-15
Persistent hyperplastic primary
vitreous
Organized vitreous hemorrhage
Falciform
fold
Retinal detachment
Retinoschisis
Retinopathy of prematurity
High
myopia
Coloboma
Medullated nerve
fibers
Chorioretinitis
Coat’s
disease
Familial exudative vitreoretinopathy
Retinoblastoma
Reticulum cell sarcoma
Astrocytoma
Glioma
Hemangioma
Norrie’s disease
Retinal dysplasia
Incontinentia pigmenti |
| Cataract: can be congenital or acquired, usually
causes blurred vision and glare. Persistent hyperplastic primary vitreous:
PHPV is a congenital condition
caused by failure of the normal regression of the primary vitreous. It is
usually associated with unilateral vision loss; Norrie’s disease also involves
deafness and mental retardation.
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Organized vitreous hemorrhage: vitreous hemorrhage is usually secondary
to a neovascular membrane or to a retinal tear. Patients may complain of a red
haze, blurred vision, or floaters. As it starts to resolve, color changes to
yellow then white and some fibrous sheets may persist. A B-scan is usually
diagnostic and vitrectomy is usually required.
Falciform fold: appears as a white fold in the retina that extends to the
optic disc. Routine monitoring of the patient is needed.
Retinal detachment: risk factors include trauma and surgery, vitreous
detachment, high myopia, retinal breaks or tears, retinal vascular disease, and
history of detachment in the other eye. symptoms include flashes of light,
floaters, curtain-like decrease in vision. Retinal detachments can be
rhegmatogenous, tractional, or exudative. When central they may cause leukocoria.
Retinopathy of prematurity: occurs in premature, low-birth-weight infants
maintained on oxygen therapy. Signs include neovascularization, fibrous bands,
retinal detachments and vitreous hemorrhage. When advanced leukocoria can be
present.
High myopia: progressive bilateral disease with complications such as
retianl detachment, staphylomas, and retinal pigment epithelium degeneration.
Coloboma: congenital condition caused by incomplete closure of the the
fetal fissure. Degree of visual loss related to area affected (iris, retina,
choroid, or optic nerve head)
Medullated nerve fibers: congenital anomaly caused by myelination of the
retinal nerve fibers and usually asymptomatic. When large areas are involved it
can cause leukocoria.
Chorioretinitis: posterior
uveitis, rarely painful but my be associated
with blurred vision or scotoma depending on location and extent. Leukocoria can
be due to excessive accumulation of debris or to the formation of large
chorioretinal scars.
Coat’s disease: typically a unilateral condition found in young boys.
It is characterized by retinal telengiectasia and aneurysms that may cause
exudative retinal detachments.
Retinoblastoma: most common primary, malignant, intraocular tumor of childhood but still a
rare tumor. Vast majority become apparent before age of 3yrs. It results from
malignant transformation of primitive retinal cells before final
differentiation. Presentation is most commonly(60%) with leukocoria and
strabismus; other presentations include secondary glaucoma, anterior segment
invasion, orbital inflammation, proptosis, metastasis, and through detection on
routine exam.
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