Ehlers-Danlos syndrome, procollagen proteinase deficient

Common Name(s)

Ehlers-Danlos syndrome, procollagen proteinase deficient

Arthrochalasia-type EDS is distinguished from other types of EDS by the frequency of congenital hip dislocation and extreme joint laxity with recurrent joint subluxations and minimal skin involvement ({2:Byers et al., 1997}; {6:Giunta et al., 2008}). Genetic Heterogeneity of Arthrochalasia-type Ehlers-Danlos Syndrome See EDSARTH2 ({617821}), caused by mutation in the COL1A2 gene ({120160}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Ehlers-Danlos syndrome, procollagen proteinase deficient" 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.
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The terms "Ehlers-Danlos syndrome, procollagen proteinase deficient" 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.