Scleredema
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Learn About Scleredema

What is the definition of Scleredema?
Scleredema is a form of cutaneous mucinosis, a diverse group of rare skin conditions that are characterized by an accumulation of mucin (a jelly-like complex carbohydrate substance) in the skin. Signs and symptoms of this condition include hardening and thickening of the skin which may restrict movement. Skin in affected areas may be red or brown and often has an 'orange-skin' appearance. In some cases, Scleredema resolves spontaneously on its own, while in other affected people, the condition persists for long periods of time.
What are the alternative names for Scleredema?
  • Scleredema
  • Buschke's scleredema
  • Scleredema adultorum
  • Scleredema adultorum of Buschke
  • Scleredema diabeticorum
  • Scleredema diabeticorum of Buschke
Who are the top Scleredema Local Doctors?
Elite in Scleredema
Elite in Scleredema
Milan, IT 

Franco Rongioletti practices practicing medicine in Milan, Italy. Mr. Rongioletti is rated as an Elite expert by MediFind in the treatment of Scleredema. He is also highly rated in 35 other conditions, according to our data. His clinical expertise encompasses Scleredema, Scleromyxedema, Papular Mucinosis, and Granuloma Annulare.

Elite in Scleredema
Elite in Scleredema
Buochs, NW, CH 

Ahmad Jalili practices practicing medicine in Buochs, Switzerland. Mr. Jalili is rated as an Elite expert by MediFind in the treatment of Scleredema. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Scleredema, Scleromyxedema, Papular Mucinosis, and Psoriasis.

 
 
 
 
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Elite in Scleredema
Elite in Scleredema
Paris, FR 

Jean-david Bouaziz practices practicing medicine in Paris, France. Bouaziz is rated as an Elite expert by MediFind in the treatment of Scleredema. They are also highly rated in 27 other conditions, according to our data. Their clinical expertise encompasses Scleredema, Scleromyxedema, Papular Mucinosis, Bone Marrow Transplant, and Kidney Transplant.

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Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center