Osteochondrodysplasia Research Paper

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Osteochondrodysplasia is a group of unusual hereditary disorders of the bone, connective tissue, or cartilage. In this disorder growth and evolution of cartilage, bone, and connective tissue are impaired. Osteochondrodysplasias can be passed down by the parent to the offspring. This disorder causes the skeleton to flourish abnormally and the results can lead to dwarfism. The chances in someone having osteochondrodysplasia is one in every 4000 to 5000 births. This disorder is not developed as growing older you are born with it.

HISTORY

Osteochondrodysplasia has not been updated since the year 2010. Back in the year 1982 was when one of the most current discoveries took place. The disorder was found on siblings and two other people. More than half of the cases of osteochondrodysplasia reported came from Mexico. During a 15 year period in the hospital of Brigham and Women's Hospital 49 out of 126000 births with the disease of osteochondrodysplasia were reported in Boston. In humans the possibility of someone being born with this disorder is one in every 4000-5000 births in the United States.
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If adult and does not reach a height compared to other people's height their age, this could be a sign. Shorter than the normal. Some non visible sign can be bone and chest deformity also respiratory failure. Symptoms related to Osteochondrodysplasia are not really common it is mainly based on signs.

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