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Posts Tagged ‘Bone disease’

Inflammatory Fibrous Hyperplasia and Getting SSI or SSDI

Thursday, December 29th, 2011

Inflammatory fibrous hyperplasia is a chronic (continuing, ongoing) bone disease that is evidenced by a part of your bone developing abnormally. Scar-like (fibrous) tissue starts to replace and take the position of normal bone tissue. With the growth of your bone, the softer fibrous tissue keeps expanding, which leads to your bone becoming weakened by this process.

Deformity may occur in your bone that is infected by inflammatory fibrous hyperplasia. If deformity does develop, it will then increase the possibility of a fracture (break) occurring in your bone that has been affected. Do you have a severe case of inflammatory fibrous hyperplasia. If this is the case, you may be eligible to receive some form of social security disability benefits like SSI or SSDI. A smart move on your part would be to get in touch with one of the social security attorneys at socialsecurityhome.com to check this out. The social security attorneys at socialsecurityhome.com stand ready to assist you in obtaining all of the disability benefits that are rightfully yours.

Inflammatory fibrous hyperplasia is believed to begin before you are born. However, you may not realize that you are affected by inflammatory fibrous hyperplasia until you reach childhood, adolescence or adulthood.

About 7% of all benign bone tumors are due to this type of  hyperplasia. Your upper arm bone, skull, thighbone, shinbone and pelvis are the areas of your body where the disease occurs most often, but inflammatory fibrous hyperplasia may take place in any bone in your body.

In most cases, inflammatory fibrous hyperplasia involves only one of your bones. In these instances, it is known as monostotic inflammatory fibrous hyperplasia. When the disease affects two or more of your bones, it is called polystotic inflammatory fibrous hyperplasia. This form of the disease may affect two of your bones in the same limb or  several bones throughout your skeleton.

Men and women are affected equally by this. It also seems to affect all races equally.

Inflammatory fibrous hyperplasia is caused by a faulty (mutated) gene that has to do with your cells that produce bone. However, what causes this gene to become faulty is unknown.

What science does know is that inflammatory fibrous hyperplasia is neither inherited or passed down from parent to child. There are also no known environmental or dietary factors that lead to inflammatory fibrous hyperplasia.

Inflammatory fibrous hyperplasia is a disease that has no known cause. It develops spontaneously. This means that it does not result from another condition nor is it related to another disorder.

You might not have any signs and symptoms at all if your inflammatory fibrous hyperplasia is mild. If the disease is severe, however, you may experience several signs and symptoms. Some of these are:

  • Bone deformities
  • Problems with being able to walk
  • Bone sores (lesions)
  • Bone pain that grows worse with any type of activity but gets better when you rest
  • Pigmentation (an unusual skin color)
  • Bone fractures (breaks)
  • Problems with your endocrine gland
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Brittle Bone Disease and Receiving Social Security Disability

Tuesday, September 13th, 2011
X-ray of U.S. girl, age 16 years 8 months, wit...

Image via Wikipedia

Brittle bone disease is a skeletal disease that is evidenced by very fragile bones that fracture easily. These broken bones often take place under loads that normal bones stand up under without difficulty.

Brittle bone disease is a connective tissue disease. It results from a malfunction in your body’s production of the protein collagen. With brittle bone disease, the amount of the collagen that is made by your body is too little, or the quality is too poor.

Brittle bone disease is a fairly rare disease. Somewhere between 20,000 and 50,000 people in the United States are affected by this disease. Brittle bone disease develops with equal frequency among all ethnic and racial groups and among women and men.

There are four main types of brittle bone disease. Type I is the mildest and most common form of the disease. Signs and symptoms of Type I include:

Ÿ  Scoliosis (curvature of the spine)

Ÿ  Triangular-shaped face

Ÿ  Fragile bones

Ÿ  Hearing loss beginning in your 20s

Ÿ  Thin, smooth skin

Ÿ  Low muscle tone

Ÿ  Brittle teeth

Ÿ  Loose joints

Ÿ  Blue sclerae (whites of the eye).

Type II, brittle bone disease accounts for about 10% of the people with this disease.

This is the most severe form of the disease. This type of brittle bone disease often causes death at or shortly after birth.

About 20% of the people with brittle bone disease have Type III. People with this form of the disease frequently have 100 fractures by the time they reach puberty. Signs and symptoms of Type III are:

Ÿ  Sclera that have a purple, gray or blue tint

Ÿ  Curvature of the spine (scoliosis)

Ÿ  Loose joints

Ÿ  Possible respiratory problems

Ÿ  Soft bones that bend, as well as break, easily

Ÿ  Triangular-shaped face

Ÿ  Possible hearing loss

Ÿ  Barrel-shaped rib cage

Ÿ  Poor tooth development that often causes your teeth to be brittle and discolored

Ÿ  Short stature

Ÿ  Poor muscle development.

 

The severity of Type IV is somewhere between Type I and Type III. Breaks usually take place before puberty with the exception of women after menopause. Some of the signs and symptoms of brittle bone disease Type IV include:

Ÿ  Below average height

Ÿ  Mild to moderate bone deformity

Ÿ  Easily overstretched, loose joints

Ÿ  Scoliosis (curvature of the spine)

Ÿ  Barrel-shaped ribcage

Ÿ  Possible hearing loss

Ÿ  Triangular-shaped face

Ÿ  Possible brittle teeth.

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