Bardet-Biedl Syndrome – A Rare Cause of Cardiomyopathy.

dc.contributor.authorYadav, Dinesh Kumar
dc.contributor.authorBeniwal, Mukesh Kumar
dc.contributor.authorJain, Aditi
dc.date.accessioned2016-01-05T10:53:23Z
dc.date.available2016-01-05T10:53:23Z
dc.date.issued2013-06
dc.description.abstractBardet-Biedl syndrome (BBS) is a rare autosomal recessive condition characterized by retinitis pigmentosa, polydactyly, obesity, learning disabilities, hypogonadism and renal anomalies. Cardiomyopathy in association with BBS has previously being reported only twice in literature. We report a case of a patient presenting with features of cardiomyopathy, who was subsequently diagnosed to have BBS.en_US
dc.identifier.citationYadav Dinesh Kumar, Beniwal Mukesh Kumar, Jain Aditi. Bardet-Biedl Syndrome – A Rare Cause of Cardiomyopathy. Indian Pediatrics. 2013 June; 50(6): 599-601.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/169857
dc.language.isoenen_US
dc.source.urihttps://www.indianpediatrics.net/june2013/june-599-601.htmen_US
dc.subjectBardet-Biedl syndromeen_US
dc.subjectCardiomyopathyen_US
dc.titleBardet-Biedl Syndrome – A Rare Cause of Cardiomyopathy.en_US
dc.typeArticleen_US
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