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https://hdl.handle.net/11499/6110
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Özdemir, Özmert M.A. | - |
dc.contributor.author | Kılıç, İlknur | - |
dc.contributor.author | Küçüktaşçı, Kazım | - |
dc.contributor.author | Gürses, Dolunay | - |
dc.contributor.author | Karaca, Abdullah | - |
dc.contributor.author | Oto, Murat | - |
dc.contributor.author | Çetin, Gökhan Ozan | - |
dc.date.accessioned | 2019-08-16T12:04:16Z | |
dc.date.available | 2019-08-16T12:04:16Z | |
dc.date.issued | 2011 | - |
dc.identifier.issn | 2146-3123 | - |
dc.identifier.uri | https://hdl.handle.net/11499/6110 | - |
dc.identifier.uri | https://doi.org/10.5174/tutfd.2009.03070.1 | - |
dc.description.abstract | Neonatal thrombosis is a serious event that can cause mortality or severe morbidity. Although catheters are the most common cause of neonatal thrombosis, spontaneous events can also occur. Arterial thrombosis is very rare and accounts for approximately half of all thrombotic events in neonates. Genetic prothrombotic risk factors may affect the occurence of neonatal thrombosis. In this report, a case of left brachial, radial, and ulnar arterial thrombosis associated with methylene-tetrahydrofolate reductase (MTHFR) gene C677T and A1298C polymorphism heterozygosity is presented. Plasma homocysteine level and other prothrombotic components were normal. Standard heparin, aspirin, vitamin B12, B6 and folic acid were initiated for treatment. However, the left arm of the patient was amputated at the shoulder because its capillary stream could not be observed. We suggest that MTHFR gene C677T and A1298C polymorphism heterozygosity might be investigated in neonates with congenital arterial thrombosis in spite of normal serum homocysteine levels. © Trakya University Faculty of Medicine. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Galenos Publishing House | en_US |
dc.relation.ispartof | Balkan Medical Journal | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Congenital arterial thrombosis | en_US |
dc.subject | Methylene-tetrahydrofolate reductase gene polymorphsim | en_US |
dc.subject | acetylsalicylic acid | en_US |
dc.subject | cyanocobalamin | en_US |
dc.subject | folic acid | en_US |
dc.subject | heparin | en_US |
dc.subject | pyridoxine | en_US |
dc.subject | arm amputation | en_US |
dc.subject | artery thrombosis | en_US |
dc.subject | article | en_US |
dc.subject | brachial artery | en_US |
dc.subject | capillary flow | en_US |
dc.subject | case report | en_US |
dc.subject | congenital brachial arterial thrombosis | en_US |
dc.subject | congenital disorder | en_US |
dc.subject | congenital radial arterial thrombosis | en_US |
dc.subject | congenital ulnar arterial thrombosis | en_US |
dc.subject | gene | en_US |
dc.subject | genetic association | en_US |
dc.subject | genetic polymorphism | en_US |
dc.subject | heterozygosity | en_US |
dc.subject | human | en_US |
dc.subject | methylene tetrahydrofolate reductase gene | en_US |
dc.subject | newborn | en_US |
dc.subject | radial artery | en_US |
dc.subject | ulnar artery | en_US |
dc.title | Congenital arterial thrombosis in newborn: A case report | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 28 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.startpage | 331 | |
dc.identifier.startpage | 331 | en_US |
dc.identifier.endpage | 334 | en_US |
dc.identifier.doi | 10.5174/tutfd.2009.03070.1 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopus | 2-s2.0-80053357076 | en_US |
dc.identifier.wos | WOS:000295492900023 | en_US |
dc.identifier.scopusquality | Q3 | - |
dc.owner | Pamukkale University | - |
item.grantfulltext | open | - |
item.openairetype | Article | - |
item.languageiso639-1 | en | - |
item.fulltext | With Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. 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: | Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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