Larsen syndrome, dominant type

Common Name(s)

Larsen syndrome, dominant type

Larsen syndrome is characterized by numerous joint dislocations at birth, flexible joints, and a distinctive appearance to the face, hands and feet. Larsen syndrome can be inherited in either an autosomal dominant or autosomal recessive pattern. Changes in the FLNB gene cause the autosomal dominant form of Larsen syndrome.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Larsen syndrome, dominant type" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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