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H Factor Deficiency: A Case with an Atypical Presentation

dc.contributor.authorRocha, AP
dc.contributor.authorBorges, M
dc.contributor.authorNeves, C
dc.contributor.authorNeves, JF
dc.date.accessioned2019-04-10T09:29:56Z
dc.date.available2019-04-10T09:29:56Z
dc.date.issued2019-02-28
dc.description.abstractWe report a case of an 18-month-old boy with H factor deficiency with atypical presentation: recurrent acute otitis media and several maternal family members with autoimmune disorders (vitiligo, thyroiditis and immune trombocytopenia). Blood tests revealed low C3 and AH50, as well as low properdin and H factor. I factor was normal. CFH gene molecular test confirmed the H factor deficiency diagnosis. This child had none of the typical manifestations of this disorder, namely Neisseria meningitidis infection or renal disease (glomerulonephritis and atypical haemolytic uremic syndrome). Autoimmune family history and correct interpretation of blood tests' results were crucial for this diagnosis.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationActa Med Port. 2019;32(2):158-161pt_PT
dc.identifier.doi10.20344/amp.10301pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/3247
dc.language.isoporpt_PT
dc.peerreviewedyespt_PT
dc.publisherCentro Editor Livreiro da Ordem dos Médicospt_PT
dc.subjectComplement Factor Hpt_PT
dc.subjectImmunologic Deficiency Syndromespt_PT
dc.subjectOtitis Mediapt_PT
dc.subjectChildpt_PT
dc.subjectHDE PEDpt_PT
dc.titleH Factor Deficiency: A Case with an Atypical Presentationpt_PT
dc.title.alternativeDéfice de Fator H: Um Caso com Apresentação Atípicapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage161pt_PT
oaire.citation.issue2pt_PT
oaire.citation.startPage158pt_PT
oaire.citation.volume32pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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