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Treatment options depend on the severity of the condition. For children under the age of two years old whose vision is affected by the cataracts in both eyes, surgical options include intraocular lens implantation or a lensectomy. [2] Congenital cataracts are considered to be a significant cause of childhood blindness.
Childhood cataract is cataract that occurs at birth or in childhood. [1] It may be congenital or acquired. Congenital cataracts are defined as the presence of lens opacification during childhood. [2] About 1.14 million children in the world are blind. [3] Cataracts are the leading cause of blindness in children. [4]
Bilateral cataracts in an infant due to congenital rubella syndrome. Signs and symptoms vary depending on the type of cataract, though considerable overlap occurs. People with nuclear sclerotic or brunescent cataracts often notice a reduction of vision. Nuclear cataracts typically cause greater impairment of distance vision than of near vision.
A cataract is an opacity that develops in the crystalline lens of the eye. [9] The word cataract literally means, "curtain of water" or "waterfall" as rapidly running water turns white, so the term may have been used metaphorically to describe the similar appearance between mature ocular opacities and water fall.
Congenital cataract is a lens transparency disorder that occurs at birth or soon after. It is a leading cause of treatable vision loss or visual impairment in children. [2] A cataract is a clouding of the eye's lens. and is caused by a disruption in the normal structure or function of the lens protein, resulting in opacity. [3]
Oculocerebrorenal syndrome (also called Lowe syndrome) is a rare X-linked recessive disorder characterized by congenital cataracts, hypotonia, intellectual disability, proximal tubular acidosis, aminoaciduria and low-molecular-weight proteinuria.
Persistent fetal vasculature (PFV), also known as persistent fetal vasculature syndrome (PFVS), and until 1997 known primarily as persistent hyperplastic primary vitreous (PHPV), [1] is a rare congenital anomaly which occurs when blood vessels within the developing eye, known as the embryonic hyaloid vasculature network, fail to regress as they normally would in-utero after the eye is fully ...
Leukocoria is a medical sign for a number of conditions, including Coats disease, congenital cataract, corneal scarring, melanoma of the ciliary body, [2] Norrie disease, ocular toxocariasis, persistence of the tunica vasculosa lentis (PFV/PHPV), retinoblastoma, and retrolental fibroplasia.