BRIEF SCENERIO OF CORNEAL DYSTROPHY AND ITS RARE CONG ASSOCIATIONS

CUROFY EXPERT CASE FOR DISCUSSION RARE AND INTERESTING CASE OF BILTERAL CONG CORNEAL DYSTROPHY WITH RARE ASSOCIATED CONG LE ANT STAPHYLOMA CORNEAL DYSTROPHY IS A RARE DISORDER THOUGHT TO BE DEPOSITION OF SOME UNKNOWN SUBSTANCE IN THE CORNEAL STROMA CAUSE NOT KNOWN HOWEVER HEREFOFAMILIAL FACTOR IS IMPORTANT DIFFERENCE BETWEEN CORNEAL DYSTROPHY AND CORNEAL DEGENERSTION IS THAT CORNEAL DYSTROPHY IS A BILTERAL CONDITION OF HEROFOFAMALIAL ENTITY WHEREAS CORNEAL DEGENERSTION IS UNILATERAL CONDITION OF NON HEREDETARY ORIGIN OTHER CORNEAL DYSTROPHYIES ARE GRANULAR MACULAR LATTICE ARCUS SENALES ARCUS JVENALIS MORANS ULCER HASLE HANLE BODIES FUCKS CORNEAL DYSTROPHY V K C PTERYGIUM ASDOCIATED CONDITIONS ASSOCIATED WITH CONG CORNEAL DYSTROPHIES ARE CONG GLAUCOMA KERSTACONUS ANT STAPHYLOMA CONG ABSENCE OF DESTMETS MEMBRANE C H E D DEAFNESS K C SICCA MEDULLATED OPTIC NERVE FIBERS PTOSIS UNLID CONJUCTIVAL XEROSIS CLINICALLY BILATERAL CONG CENTRAL SYMETRICAL CORNEAL OPACITY WITH ABSENCE OF DEEP VASCULARISATION AND IMPAIRED CORNEAL SENSATION IS CORNEAL DYSTROPHY UNLESS PROVED OTHERWISE CLINICAL DEFINITION OF CORNEAL DYSTROPHY LESIONS IN THE CORNEA OF UNKNOWN ATEOLOGY WHICH MAY MANIFEST EITHER AT BIRTH OR AT 2ND OR 3RD DECADE OF LIFE MAY REMAINE STATIONARY OR PROGRESSIVE HAS GOT STRONG HEREDOFAMILAL TENDENCY

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