What is another word for Schuller-christian Disease?
Pronunciation: [ʃˈʌləkɹˈɪst͡ʃən dɪzˈiːz] (IPA) 
Schuller-Christian Disease, also known as lipoid proteinosis, is a rare autosomal recessive disorder characterized by the deposition of hyaline material in various tissues of the body. The disease commonly affects the skin, mucous membrane, and internal organ systems, leading to a range of symptoms such as hoarseness, skin lesions, thickening of the skin, and cognitive impairment. Although the term "Schuller-Christian Disease" is commonly used, there are several synonyms for the condition, including Urbach-Wiethe Disease, hyalinosis cutis et mucosae, and lipoglycoproteinosis. While there is currently no cure for the disease, treatment options include management of symptoms and supportive care.
