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Bhaskar–Jagannathan syndrome

FieldValue
specialtyGenetic disorder

Bhaskar–Jagannathan syndrome is an extremely rare genetic disorder and there is a limited amount of information related to it. Similar or related medical conditions are arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones.

Signs and symptoms

Bhaskar–Jagannathan has symptoms such as long fingers, thin fingers, poor balance, incoordination, high levels of amino acids in urine, cataracts during infancy, and ataxia. Ataxia, which is a neurological sign and symptom made up of gross incoordination of muscle movements and is a specific clinical manifestation

Diagnosis

There are three different ways to diagnose Bhaskar–Jagannathan. This disorder may be diagnosed by a urine test, a blood test, and an X-ray of the eyes or other body parts.

Treatment

Treatment for this rare genetic disorder can be physical therapy, there have been antibiotics found to be effective, and surgery has been found to be another solution.

References

References

  1. Bhaskar Jagannathan Syndrome (2012). In IAMUNWELL. Retrieved April 5, 2012, from http://www.iamunwell.com/Diseases-Alphabet-B/bhaskar-jagannathan-syndrome.html {{Webarchive. link. (2012-08-13)
  2. Bhaskar Jagannathan syndrome . RD - Right Diagnosis, 1 Feb. 2012. Web. 5 Apr. 2012. http://www.rightdiagnosis.com/b/bhaskar_jagannathan_syndrome/intro.htm#whatis
Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

congenital-disorders genetic-disorders-with-no-omim rare-syndromes syndromes-affecting-the-nervous-system syndromes-affecting-the-eye
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