Paget’s Disease:
Paget’s disease is a chronic bone condition affecting remodeling at the microscopic level resulting in the rate of bone remodeling outbalancing bone breakdown – this leads to abnormally enlarged bone growths with impaired structural integrity compared to bone with a normal turnover rate.
Older Caucasians tend to be at higher risk of developing Paget’s disease, affecting males slightly more than females with the exact cause remaining under investigation. Bones more commonly at risk include the skull, spine, pelvis, femur and humerus.
Osteomalacia:
Often as a result of Vitamin D deficiency, Osteomalacia entails a bone softening effect, subject to both bending and breaking, as a direct result of poor calcium absorption and bone mineralization.
As Vitamin D uptake can also be affected by various conditions such as Celiac or diseases of the liver and kidneys, treatments can vary but will often involve Vitamin D and calcium supplementation. As sun exposure is an important source of Vitamin D, world regions with cooler climates or with traditional body covering practices are often at risk.
Osteogenesis Imperfecta:
A genetically obtained disorder drawing from a collagen mutation, OI – otherwise known as ‘brittle bone disease’ results in a malformed skeletal structure often accompanied by blue tinting in the eye sclerae and opal tinged teeth.
As there is currently no cure for this genetic condition, prosthetic (metal) reinforcements and treatments such as bisphosphonate therapy are amongst the most common courses of action.