Publication:
Case report: Pediatric age onset CNTN1 antibody-associated neuropathy with nephropathy and literature review

dc.contributor.coauthorEltutan, Ceyda Bayraktar
dc.contributor.coauthorRinaldi, Simon
dc.contributor.coauthorAksu, Bagdagul
dc.contributor.coauthorGenc, Hulya Maras
dc.contributor.coauthorYildiz, Edibe Pembegul
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.kuauthorVural, Atay
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2025-09-10T04:57:36Z
dc.date.available2025-09-09
dc.date.issued2025
dc.description.abstractWe present a 12-year-old boy with acute onset sensorimotor neuropathy and membranous glomerulonephritis associated with contactin-1 antibodies. This prompted us to explore the clinical characteristics of this condition and assess whether its presentation differs between pediatric and adult patients. A comprehensive search was conducted across multiple online databases, including PubMed and EMBASE, using MeSH terms such as chronic inflammatory demyelinating polyradiculopathy, acute inflammatory demyelinating polyradiculopathy , CIDP, Guillain Barre syndrome, proteinuria, nephrotic syndrome, nephropathy, renal disease, glomerulonephritis, membranous nephropathy, autoimmune nodopathies, and membranous glomerulonephritis. We reviewed publications up to October 2024 and identified 39 patients with anti-contactin associated CIDP (chronic inflammatory demyelinating polyradiculopathy) with membranous glomerulonephritis (MGN), including our case. This rare coexistence typically occurs at advanced ages, with only two pediatric cases. Clinical features were similar regardless of age at onset. We compared the onset, symptoms, progression, renal histopathology, and treatment responses between pediatric and adult patients.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessGold OA
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished Version
dc.description.volume16
dc.identifier.doi10.3389/fimmu.2025.1549363
dc.identifier.embargoNo
dc.identifier.filenameinventorynoIR06445
dc.identifier.issn1664-3224
dc.identifier.pubmed40607401
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-105009615887
dc.identifier.urihttps://doi.org/10.3389/fimmu.2025.1549363
dc.identifier.urihttps://hdl.handle.net/20.500.14288/30267
dc.identifier.wos001522174500001
dc.keywordsChronic inflammatory demyelinating polyradiculopathy
dc.keywordsMembranous glomerulonephritis
dc.keywordsAutoimmune nodopathy
dc.keywordsAnti-contactin antibody
dc.keywordsChild
dc.language.isoeng
dc.publisherFrontiers Media Sa
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofFrontiers in Immunology
dc.relation.openaccessYes
dc.rightsCC BY (Attribution)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectImmunology
dc.titleCase report: Pediatric age onset CNTN1 antibody-associated neuropathy with nephropathy and literature review
dc.typeJournal Article
dspace.entity.typePublication
person.familyNameVural
person.givenNameAtay
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relation.isOrgUnitOfPublication.latestForDiscovery91bbe15d-017f-446b-b102-ce755523d939
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