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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.
Congenital cataracts are a lens opacity that is present at birth. Congenital cataracts occur in a broad range of severity. Some lens opacities do not progress and are visually insignificant, others can produce profound visual impairment. Congenital cataracts may be unilateral or bilateral. They can be classified by morphology, presumed or ...
Even when treated, childhood cataracts may be associated with some complications. [2] About 10% to 25% of children have been diagnosed with glaucoma after cataract surgery. [2] [4] The most common complication after cataract surgery in childhood is visual axis opacification. [2] [4] Cataract surgery may be associated with decreased ...
The World Health Organization (WHO) publishes a classification of known diseases and injuries, the International Statistical Classification of Diseases and Related Health Problems, or ICD-10. This list uses that classification.
It may also include congenital cataracts. [3] The cause of this syndrome was discovered in 1999. [4] Children with this syndrome often present with a joint effusion that is cool and resistant to anti-inflammatory therapy. The arthropathy principally involves large joints such as elbows, hips, knees, and ankles.
Nance–Horan syndrome, also known as X-linked congenital cataracts and microcornea, X-linked cataract–dental syndrome, cataracts-oto-dental syndrome, cataract–dental syndrome, and mesiodens–cataract syndrome, is a rare X-linked syndrome characterized by eye and teeth abnormalities, intellectual disability, and facial deformities.
A Wisconsin man who faked his own drowning and left his wife and three children to go to Eastern Europe is in police custody, online records show.. Ryan Borgwardt, 45, was booked into the Green ...
Warburg Micro syndrome (WARBM), a Complex Hereditary Spastic Paraplegia or RAB18 Deficiency, is a rare autosomal recessive genetic disorder characterized by congenital cataract, hypotonia, spastic diplegia, intellectual or developmental disability, microcephaly, microcornea, optic atrophy, and hypogenitalism. [5]
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