Brittle Bones

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Osteogenesis Imperfecta (Brittle Bone Disease)

Justin Sutcliffe. Women face epidemic of brittle bones.

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Create a commenting name to join the debate Submit. Please try again, the name must be unique Only letters and numbers accepted. Loading comments Please try again, the name must be unique. Cancel Post. There are no Independent Premium comments yet - be the first to add your thoughts. Family histories and genetic testing can help with diagnosis, and further urine and blood tests can be done to rule out potential other causes. Osteogenesis imperfecta is impossible to cure, but people can learn to live with it.

They learn how to care for fractures and how to partake in safe exercise, like swimming. They often go through physical therapy in order to strengthen muscles and improve motor skills. Treatment may also focus on a nutritious diet and a generally healthy lifestyle. Osteoporosis is not just an adult's disease; there is such a thing as juvenile osteoporosis.

Osteogenesis Imperfecta / Brittle Bone Disease

It is most common for children ages but can hit younger children going through growth spurts, as well. There are two types of juvenile osteoporosis: secondary and idiopathic. Secondary osteoporosis can be caused by a variety of other medical conditions, such as diabetes, celiac disease, kidney disease, leukemia, and cystic fibrosis. Idiopathic osteoporosis is far rarer and there is no known cause. In general, osteoporosis is a decrease in bone mass. Some common symptoms of juvenile osteoporosis are difficulty-walking, fractures that are caused too easily, and pain in the lower body, such as in the feet or knees.

The best way to treat secondary osteoporosis is to treat the underlying condition causing the bone disorder.

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  • Osteoporosis - Symptoms and causes - Mayo Clinic!

Idiopathic osteoporosis has no known treatment, so the best things to do are provide enough calcium and vitamin D in the diet and try to prevent fractures. Vitamin D deficiency, rickets, recurrent fractures, osteogenesis imperfecta brittle bones , and osteoporosis are just a few of the bone disorders that can affect children. It is clear that they all have different causes, symptoms, and treatment, so it is important that if a bone disorder is suspected, the child be taken to a doctor to determine exactly what's wrong so the right treatment can be prescribed.

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Vitamin D Deficiency Vitamin D is an essential nutrient found in some natural foods like fish and egg yolks, but it is also made by skin that's exposed to sunlight. Rickets Rickets is a rare disorder most commonly seen in children ages months. Recurrent Fractures Recurrent fractures may be the result of other bone disorders, and they are especially problematic in children.

Brittle Bones, or Osteogenesis imperfecta OI , is a genetic disorder characterised by fragile bones that break easily.

Osteoporosis - Symptoms and causes - Mayo Clinic

A person is born with this disorder and is affected throughout his or her life time. OI is a genetic disorder of collagen, a protein which forms the framework for the bone structure. In OI the collagen may be of poor quality, or there may just not be enough to support the mineral structure of the bones. This makes the bones weak and fragile and results in the bones being liable to fracture at anytime even without trauma.

Each time a bone is broken and set it will heal in a position slightly less than perfect and the same bone may often break repeatedly. As the composition of collagen in the bone is not correct, even when there are no fractures there will be other problems connected to the condition, such as muscle weakness, hearing loss, fatigue, joint laxity, curved bones, scoliosis, blue sclerae, dentinogenesis imperfecta brittle teeth , and short stature. Restrictive pulmonary disease occurs in more severely affected people.

When there is uncertainty about the diagnosis, it is best to consult a physician who is familiar with OI. Genetic testing is available to confirm a diagnosis of OI through collagen or gene analysis—a skin sample or a blood sample are used to study the amount of Type I collagen or to do a DNA analysis.

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