Bhaskar Jagannathan Syndrome

Common Name(s)

Bhaskar Jagannathan Syndrome

Bhaskar Jagannathan syndrome is a rare genetic disorder, meaning that it is passed on from parents to children. Symptoms of Bhaskar Jagannathan syndrome include long and thin fingers, poor balance, high levels of amino acids (nutrients your body needs) in urine, cataracts (clouding of the eyes) during infancy, and ataxia. Bhaskar Jagannathan syndrome can be diagnosed using a blood test, urine test, or x-ray. Physical therapy and some antibiotics have been shown to help people affected by Bhaskar Jagannathan syndrome. Talk with your doctor to find the best treatment if you or a loved one has been diagnosed with Bhaskar Jagannathan syndrome.

Source: Advocacy organizations associated with the condition.

 

Advocacy and Support Organizations

 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Bhaskar Jagannathan Syndrome" 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 "Bhaskar Jagannathan Syndrome" returned 0 free, full-text research articles on human participants.

Reviews from the PubMed Database

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The terms "Bhaskar Jagannathan Syndrome" 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.