Eyelid papules due to lipoid proteinosis in skin of colour (LPR-patient1)
Keywords: Autosomal recessive condition, Bilateral eyes, Eyelid beading, Eyes, Face, Genetic and congenital disorder, Hyalinosis cutis et mucosae, Lipoglycoproteinosis, Lipoid proteinosis cutis et mucosae, Moniliform blepharosis, Skin of colour, Urbach-wiethe disease
Lipoid proteinosis is a rare genodermatosis characterised by the progressive deposition of amorphous hyaline material in the skin, mucosae, and internal organs. It often presents with hoarseness in early childhood, skin and mucosal changes, and neurological and psychiatric symptoms.
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Source: Carol Lobo
