Spondyloepimetaphyseal dysplasia Sponastrime type

Common Name(s)

Spondyloepimetaphyseal dysplasia Sponastrime type

Spondyloepimetaphyseal dysplasia Sponastrime type is a rare hereditary growth disorder which affects bone growth. Affected individuals typically have short stature, relatively short limbs, and abnormal facial structure. Facial abnormalities include a low nasal bridge, a large forehead, and incomplete development of the midface (midface hypoplasia). Although many affected individuals have normal intelligence, some cases have been reported with intellectual disability or mental retardation.

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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 "Spondyloepimetaphyseal dysplasia Sponastrime type" 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 "Spondyloepimetaphyseal dysplasia Sponastrime type" 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 "Spondyloepimetaphyseal dysplasia Sponastrime type" 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.