Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/56669
Full metadata record
DC FieldValueLanguage
dc.contributor.authorÖzdemir, Özmert Muhammet Ali-
dc.contributor.authorTurgut, Musa-
dc.contributor.authorSönmez Demir, Gülay-
dc.contributor.authorUzunlu, Osman-
dc.contributor.authorErgin, Hacer-
dc.date.accessioned2024-02-24T14:31:24Z-
dc.date.available2024-02-24T14:31:24Z-
dc.date.issued2023-
dc.identifier.issn1302-7123-
dc.identifier.issn1308-5123-
dc.identifier.urihttps://doi.org/10.14744/SEMB.2022.02359-
dc.identifier.urihttps://hdl.handle.net/11499/56669-
dc.description.abstractHolt-Oram syndrome (HOS) is characterized by upper-limb defects and congenital heart malformation, and its prevalence is very rarely. Mature cystic teratoma is the most common tumor seen in neonates and its most common location is sacrococcygeal region. Diagnosis of a sacrococcygeal teratoma should be confirmed by pathology. Surgical resection is the mainstay therapeutic approach of this tumor. Some malformations such as genitourinary system, musculoskeletal anomalies, neural defects, cardiovascular anomalies, and pulmonary disorders associated with this tumor have been reported. Herein, we reported a male neonate diagnosed with HOS associated with sacrococcygeal teratoma. To our knowledge, it has been not reported a case with HOS associated with sacrococcygeal teratoma. Patients with sacrococcygeal teratomas (SCTs) may have multiple and extreme congenital abnormalities; therefore, patients with SCTs should be carefully evaluated clinically, laboratory, and radiologically and it should be also considered that HOS may accompany them.en_US
dc.language.isoenen_US
dc.publisherKare Publen_US
dc.relation.ispartofMedical Bulletin of Sisli Etfal Hospitalen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHolt-Oram syndromeen_US
dc.subjectnewbornen_US
dc.subjectsacrococcygeal regionen_US
dc.subjectteratomaen_US
dc.titleHolt-Oram Syndrome with Sacrococcygeal Teratoma - A Rare Associationen_US
dc.typeArticleen_US
dc.identifier.volume57en_US
dc.identifier.issue4en_US
dc.identifier.startpage563en_US
dc.identifier.endpage566en_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.14744/SEMB.2022.02359-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid38268646en_US
dc.identifier.wosWOS:001136225000010en_US
dc.institutionauthor-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairetypeArticle-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.01. Surgical Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Files in This Item:
File SizeFormat 
SETB-02359-CASE_REPORT-TURGUT[A].pdf449.55 kBAdobe PDFView/Open
Show simple item record



CORE Recommender

WEB OF SCIENCETM
Citations

1
checked on Dec 3, 2024

Page view(s)

44
checked on Aug 24, 2024

Download(s)

14
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.