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https://hdl.handle.net/11499/56669
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DC Field | Value | Language |
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dc.contributor.author | Özdemir, Özmert Muhammet Ali | - |
dc.contributor.author | Turgut, Musa | - |
dc.contributor.author | Sönmez Demir, Gülay | - |
dc.contributor.author | Uzunlu, Osman | - |
dc.contributor.author | Ergin, Hacer | - |
dc.date.accessioned | 2024-02-24T14:31:24Z | - |
dc.date.available | 2024-02-24T14:31:24Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 1302-7123 | - |
dc.identifier.issn | 1308-5123 | - |
dc.identifier.uri | https://doi.org/10.14744/SEMB.2022.02359 | - |
dc.identifier.uri | https://hdl.handle.net/11499/56669 | - |
dc.description.abstract | Holt-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.iso | en | en_US |
dc.publisher | Kare Publ | en_US |
dc.relation.ispartof | Medical Bulletin of Sisli Etfal Hospital | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Holt-Oram syndrome | en_US |
dc.subject | newborn | en_US |
dc.subject | sacrococcygeal region | en_US |
dc.subject | teratoma | en_US |
dc.title | Holt-Oram Syndrome with Sacrococcygeal Teratoma - A Rare Association | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 57 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 563 | en_US |
dc.identifier.endpage | 566 | en_US |
dc.department | Pamukkale University | en_US |
dc.identifier.doi | 10.14744/SEMB.2022.02359 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 38268646 | en_US |
dc.identifier.wos | WOS:001136225000010 | en_US |
dc.institutionauthor | … | - |
item.languageiso639-1 | en | - |
item.grantfulltext | open | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.fulltext | With Fulltext | - |
item.openairetype | Article | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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File | Size | Format | |
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SETB-02359-CASE_REPORT-TURGUT[A].pdf | 449.55 kB | Adobe PDF | View/Open |
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