Ophthalmic Presentation of Lipoid Proteinosis in Iraqi Siblings: Case Report

The present study highlights the clinical manifestations, progression, and conservative treatment of lipoid proteinosis in two patients from an Iraqi family. An abnormal buildup glycoprotein numerous organs is known as (LP), autosomal recessive disorder. Hoarseness speech, skin lesions, scars, papules that bead up around eyelids, are all potential symptoms. Epilepsy neuropsychiatric diseases can result calcifications brain tissue. In this paper, cases 13 15-yearold family siblings (born to consanguineous parents) reported. They were presented Ibn Al-Haithem Hospital with hoarseness characteristic symptomatic moniliform eyelid lesions. Biopsy confirmed diagnosis. Though ocular involvement LP rare, ophthalmologists may encounter diverse complications. With exception possible acute respiratory or neurological sequelae, disease runs a slowly progressive but otherwise benign course. rarity motivated report.