What does CED mean in DISEASES
Camurati-Engelmann Disease (CED) is an inherited disorder that affects the bones, joints and connective tissue. It is a rare condition ~ with approximately 200 cases reported worldwide ~ and is usually diagnosed in childhood or early adulthood.
CED meaning in Diseases in Medical
CED mostly used in an acronym Diseases in Category Medical that means Camurati Engelmann Disease
Shorthand: CED,
Full Form: Camurati Engelmann Disease
For more information of "Camurati Engelmann Disease", see the section below.
Essential Questions and Answers on Camurati Engelmann Disease in "MEDICAL»DISEASES"
What causes CED?
CED is caused by mutations in the prolyl 3-hydroxylase 1 gene. This gene encodes for an enzyme which plays an important role in the production of proteins within connective tissue, cartilage and bone. Mutations in this gene disrupt the proteins' formation and cause abnormal changes to occur within these tissues.
What are some of the symptoms of CED?
Common symptoms of CED include thickening and hardening of bones, pain and stiffness in joints, joint deformities, delayed walking ability, muscle weakness, curvature of the spine and fatigue.
How is CED treated?
Treatment for CED focuses on relieving symptoms; this may involve physical therapy, exercise programs, use of walking braces or splints, medication (e.g., for pain relief) and surgery (e.g., corrective surgery to correct joint deformities).
Final Words:
CED is a rare disorder that usually appears in childhood or early adulthood; its associated symptoms can be managed through physical therapy, exercise programs or surgical interventions when necessary. A firm diagnosis requires genetic testing to confirm mutations in the prolyl 3-hydroxylase 1 gene; only around 200 cases have been reported so far worldwide.