[Urbach-Wiethe syndrome]
- PMID: 130880
[Urbach-Wiethe syndrome]
Abstract
The "Urbach-Wiethe syndrom" is an hereditary disease which start during early childhood, distinguishable by a lipoglycoproteinosis which affects the skin, mucosae and also the eyes, with cyst formations in the lid's marginal, drusen of Bruch's membrane. Corneal opacities, and glaucoma seen to be rarer.