A cataract is any clouding of the lens of the eye. a congenital cataract is an opacity of the lens that occurs in the fetus at some time during pregnancy and is present at birth.
Causes, incidence, and risk factors
Although there are many diseases and inherited disorders that can lead to congenital cataracts, the actual incidence of congenital cataracts is low. In most patients with congenital cataract, no specific cause can be identified. This is a partial list of possible causes of congenital cataracts:
galactosemia chondrodysplasia syndrome congenital rubella syndrome
Down's syndrome (trisomy 21) Pierre-Robin syndrome familial congenital cataracts Hallerman-Streiff syndrome cerebrohepatorenal syndrome (Lowe's syndrome) Trisomy 13 Conradi syndrome Ectodermal dysplasia syndrome Marinesco-Sjogren syndrome
Signs and tests
A complete eye examination by an ophthalmologist will readily diagnose congenital cataract. The search for a possible cause may require examination by a pediatrician experienced in hereditary disorders with possible blood tests and x-rays.
Treatment
The treatment involves surgical cataract removal followed by placement of an intraocular lens (IOL). Patching to force use of the weaker eye may be required to prevent amblyopia . If an underlying disorder is found, treatment of that disorder may be needed.
Expectations (prognosis)
Cataract surgery with IOL placement is routine and usually has excellent results.
Complications
Many of the underlying diseases associated with congenital cataract have extensive involvement of multiple organs and organ systems.
Calling your health care provider
Call for an appointment with your baby's health care provider if you notice that the pupil (the normally dark part in the center of the eye) of one or both eyes appears white or cloudy.
Prevention
If you have a family history of any of the above inheritable disorders consider seeking genetic counseling.