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    GlossaryLipoid Proteinosis

    rare genetic disorder causing waxy deposits in skin and organs

    Lipoid Proteinosis, also known as Urbach-Wiethe disease, is a rare genetic disorder characterized by the abnormal deposition of a waxy, protein-rich material in the skin, mucous membranes, and various internal organs. This can lead to symptoms such as thickened skin, hoarseness, and in some cases, neurological issues due to calcifications in the brain, particularly in the medial temporal lobes.

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