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Bhaskar Jagannathan Syndrome
DefinitionDefinition of Bhaskar Jagannathan Syndrome Bhaskar Jagannathan syndrome is an extremely rare genetic disorder that is characterized by the constellation of features like arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones. When the entity was initially reported, the author raised the question if it could be a new cerebro-oculo-renal syndrome. SymptomsSymptoms of Bhaskar Jagannathan Syndrome People affected with Bhaskar Jagannathan syndrome display some delayed developmental milestones and may suffer from incoordination. Patients may also have poor balance, and possess long and thin fingers. Infants with the disease initially form cataracts early on. They may also suffer from ataxia, which is a neurological sign and symptom made up of gross incoordination of muscle movements and is an aspecific clinical manifestation (implies dysfunction of parts of the nervous system that coordinate movement, such as the cerebellum). People affected with the Bhaskar Jagannathan syndrome have an increased level of amino acids in the urine. DiagnosisDiagnosis of Bhaskar Jagannathan Syndrome The best way to diagnose the diseae is to monitor the symptoms of the disease, which can be notices after the few month of the disorder.
TreatmentTreatment of Bhaskar Jagannathan Syndrome The only effective treatment for the disease the practicing of good physiotherapy and daily exercise. However, recently various drugs including Antibiotics have also been researched for effective treatment of the Bhaskar Jagannathan Syndrome. Apart from this, surgery and operation are the other solutions. Find Diseases Alphabetically
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