A rare case of polydactyly with multiple defects

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dc.contributor.authorKumar, Sanjeeven_US
dc.contributor.authorBansal, Pradeep Kumaren_US
dc.contributor.authorIshran, Rohiten_US
dc.contributor.authorKasana, Rajendraen_US
dc.date.accessioned2020-04-09T07:43:30Z
dc.date.available2020-04-09T07:43:30Z
dc.date.issued2020-02
dc.description.abstractBardet-Biedl Syndrome (BBS) is a very rare genetically heterogenous disorder. Here is a case of 27 yr. old obese male presented with acute gastroenteritis with shock in our department. He had polydactyly in both upper limb and left lower limb, blindness since childhood, with difficult in learning and delayed onset of milestones. Patient抯 sibling (younger brother 20-year-old) also had same problems since childhood and one female baby died within few days of birth. He was having single testis. Patient was managed conservatively. The available literature on this syndrome was reviewed.en_US
dc.identifier.affiliationsDepartment of Medicine, SMS Medical College, Jaipur, Rajasthan, Indiaen_US
dc.identifier.citationKumar Sanjeev, Bansal Pradeep Kumar, Ishran Rohit, Kasana Rajendra. A rare case of polydactyly with multiple defects. International Journal of Advances in Medicine. 2020 Feb; 7(2): 334-336en_US
dc.identifier.issn2349-3925
dc.identifier.issn2349-3933
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/194594
dc.languageenen_US
dc.publisherMedip Academyen_US
dc.relation.issuenumber2en_US
dc.relation.volume7en_US
dc.source.urihttps://dx.doi.org/10.18203/2349-3933.ijam20200090en_US
dc.subjectBardet-Biedl Syndromeen_US
dc.subjectBlindnessen_US
dc.subjectHeterogenous disorderen_US
dc.subjectMilestoneen_US
dc.subjectObeseen_US
dc.subjectPolydactylyen_US
dc.titleA rare case of polydactyly with multiple defectsen_US
dc.typeJournal Articleen_US
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