Publication:
Surgical correction of a ventricular septal defect in a child with spinal muscular atrophy type 2 treated with nusinersen sodium: a case report

dc.contributor.coauthorÖztürk, Figen
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorAkçay, Ayfer Arduç
dc.contributor.kuauthorBiçer, Mehmet
dc.contributor.kuauthorKozan, Şima
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:03:19Z
dc.date.issued2023
dc.description.abstractIntroduction: Spinal muscular atrophy (SMA) is a severe, inherited neuromuscular disorder characterized by progressive muscle weakness and atrophy. Cardiac pathology co-existence is reported more frequently in the severely affected patient groups. Structural heart anomalies, mainly septal, and outflow tract defects are commonly observed pathologies. Case presentation: We herein report the case of a 23 days-old female patient with the diagnosis of spinal muscular atrophy type 2 complicated with structural heart defects. Successful pulmonary banding, and at the age of 17 months, subsequent surgical atrial and ventricular septal defect closure were performed on our patient who was under treatment of Nusinersen Sodium. Post-operative recovery was uncomplicated. Cardiac assessments were normal, and the patient was neurologically improving in her recent follow-up. Conclusion: In the literature, there are no reported cases of successful surgical repair of heart defects in spinal muscular atrophy patients. These patients can be perceived as risky surgical candidates with suboptimal postoperative recovery given the unfavorable disease prognosis of SMA in untreated patients. We report our promising experience with a SMA type 2 patient undergoing a disease-modifying medical treatment. The SMA patients under treatment may be potential candidates for successful surgical cardiac correction given their overall improved prognosis. © 2023, The Author(s).
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.indexedbyWOS
dc.description.issue1
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume18
dc.identifier.doi10.1186/s13019-023-02170-z
dc.identifier.issn1749-8090
dc.identifier.scopus2-s2.0-85147784339
dc.identifier.urihttps://doi.org/10.1186/s13019-023-02170-z
dc.identifier.urihttps://hdl.handle.net/20.500.14288/8451
dc.identifier.wos932334400001
dc.keywordsCongenital heart defects
dc.keywordsNeuromuscular disorders
dc.keywordsPulmonary banding
dc.keywordsSpinal muscular atrophy
dc.keywordsVentricular septal defect
dc.keywordsChild
dc.keywordsFemale
dc.keywordsHeart septal defects, Ventricular
dc.keywordsHumans
dc.keywordsInfant
dc.keywordsMuscular atrophy, Spinal
dc.keywordsSodium
dc.keywordsSpinal muscular atrophies of childhood
dc.keywordsNusinersen
dc.keywordsSodium
dc.keywordsCase report
dc.keywordsComplication
dc.keywordsHeart septum defect
dc.keywordsHereditary spinal muscular atrophy
dc.keywordsHuman
dc.keywordsSpinal muscular atrophy
dc.language.isoeng
dc.publisherBioMed Central Ltd
dc.relation.ispartofJournal of Cardiothoracic Surgery
dc.subjectSpinal muscular atrophy
dc.subjectNusinersen
dc.subjectMotor neurons
dc.titleSurgical correction of a ventricular septal defect in a child with spinal muscular atrophy type 2 treated with nusinersen sodium: a case report
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorAkçay, Ayfer Arduç
local.contributor.kuauthorBiçer, Mehmet
local.contributor.kuauthorKozan, Şima
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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