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Beyond Polycystic Kidney Disease

dc.contributor.authorSantos, SF
dc.contributor.authorFrancisco, T
dc.contributor.authorCordeiro, AI
dc.contributor.authorLopes, MJ
dc.date.accessioned2017-11-14T16:07:50Z
dc.date.available2017-11-14T16:07:50Z
dc.date.issued2017-10-04
dc.description.abstractTuberous sclerosis(TS) is an autosomal dominant disease caused by mutations in TSC1 and TSC2 genes. TSC2 gene is located in chromosome 16p13.3, adjacent to PKD1 gene, responsible for the autosomal dominant polycystic kidney disease. In a rare subgroup of patients, the presence of a deletion which simultaneously affects the TSC2 and PKD1 genes has been confirmed. TSC2/PKD1-Contiguous Gene Syndrome is characterised by the early appearance of autosomal dominant polycystic kidney disease in combination with several phenotypic manifestations of TS. We present a 13-year-old girl with bilateral renal cysts detected at the age of 9 months. At the age of 13, she was referred to the Dermatology Outpatients Clinic due to a facial cutaneous eruption. She presented with facial erythema, fibroadenomas with malar distribution and disseminated hypomelanotic macules, meeting the criteria for TS. TSC2/PKD1 Contiguous Gene Syndrome deletion was suspected, being later confirmed by genetic testing.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBMJ Case Rep. 2017 Oct 4;2017pt_PT
dc.identifier.doi10.1136/bcr-2017-220766pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/2804
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBMJ Publishing Grouppt_PT
dc.subjectPolycystic kidneypt_PT
dc.subjectNeuroimagingpt_PT
dc.subjectGeneticspt_PT
dc.subjectDermatologypt_PT
dc.subjectHDE PEDpt_PT
dc.subjectHSAC DERpt_PT
dc.titleBeyond Polycystic Kidney Diseasept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPage220766pt_PT
oaire.citation.volume2017pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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