Spondylometaphyseal dysplasia with dentinogenesis imperfecta

Common Name(s)

Spondylometaphyseal dysplasia with dentinogenesis imperfecta

Spondylometaphyseal dysplasia with dentinogenesis imperfecta is a type of rare hereditary disorder which affects bone growth. The condition is characterized by dwarfism, abnormal growth of long bones, loose joints, narrow chest, and tooth enamel abnormalities. The shortness in the arms and legs occurs mainly in the forearm and lower leg bones. Growth abnormalities are usually evident by the second year of life. It affects approximately 1 in 100,000 people.

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Advocacy and Support Organizations

 

Condition Specific Organizations

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Spondylometaphyseal dysplasia with dentinogenesis imperfecta" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Spondylometaphyseal dysplasia with dentinogenesis imperfecta" returned 0 free, full-text research articles on human participants.

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Spondylometaphyseal dysplasia with dentinogenesis imperfecta" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.