Carney complex variant

Common Name(s)

Carney complex variant

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Carney complex variant" 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 "Carney complex variant" returned 1 free, full-text research articles on human participants. First 3 results:

Mutation of perinatal myosin heavy chain associated with a Carney complex variant.
 

Author(s): Mark Veugelers, Michael Bressan, Deborah A McDermott, Stanislawa Weremowicz, Cynthia C Morton, C Charlton Mabry, Jean-Fran├žois Lefaivre, Alan Zunamon, Anne Destree, Jean-Marie Chaudron, Craig T Basson

Journal: N. Engl. J. Med.. 2004 Jul;351(5):460-9.

 

Familial cardiac myxomas occur in the hereditary syndrome Carney complex. Although PRKAR1A mutations can cause the Carney complex, the disorder is genetically heterogeneous. To identify the cause of a Carney complex variant associated with distal arthrogryposis (the trismus-pseudocamptodactyly ...

Last Updated: 29 Jul 2004

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Reviews from the PubMed Database

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

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.