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Crusted scaly lesions on the toe in lipoid proteinosis (LPR-patient1)
Keywords: Autosomal recessive condition, Foot, Genetic and congenital disorder, Hyalinosis cutis et mucosae, Hyperkeratotic patch, Lipoglycoproteinosis, Lipoid proteinosis cutis et mucosae, Skin of colour, Toe, Urbach-wiethe disease, Verrucous dorsal toe plaque
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