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4 Possible Causes for Partial or Total Corneal Opacification

  • Microcornea

    Symptoms INHERITANCE: Autosomal recessive HEAD AND NECK: [Eyes]; Corneal opacification, partial or total; Sclerocornea (in some patients); Cataract (in some patients); Microcornea[findzebra.com] The extent of corneal opacification prevented visualization of the anterior chamber or fundus, and the presence or absence of cataract could not be deter...[findzebra.com]

  • Other Congenital Corneal Malformations

    Symptoms INHERITANCE: Autosomal recessive HEAD AND NECK: [Eyes]; Corneal opacification, partial or total; Sclerocornea (in some patients); Cataract (in some patients); Microcornea[findzebra.com] The extent of corneal opacification prevented visualization of the anterior chamber or fundus, and the presence or absence of cataract could not be deter...[findzebra.com]

  • Aniridia

    […] changes with opacification and neovasularisation, and unusual partly pigmented cortical lens opacities (PTC mutation). ( c ) Partial absence of iris tissue (missense mutation[ncbi.nlm.nih.gov] ). ( d ) Severe aniridic keratopathy with total loss of transparency and neovasularisation of the cornea (PTC mutation). ( e ) Full iris demonstrating substantial area of[ncbi.nlm.nih.gov] […] tissue with surgical aphakia (removal of natural lens) and remnant of opaque lens capsule (CTE mutation). ( b ) Almost complete absence of iris tissue obscured by peripheral corneal[ncbi.nlm.nih.gov]

  • Congenital Cataract - Microcornea - Corneal Opacity

    PURPOSE: To investigate whether three consanguineous families from the Punjab province of Pakistan, with affected members with recessively inherited congenital cataract microcornea with corneal opacity, are genetically homogeneous. METHODS: An ophthalmic examination was performed on each family member to establish[…][ncbi.nlm.nih.gov]

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