Neonatal cerebral sinovenous thrombosis: Two cases, two different gene polymorphisms and risk factors.
Turk J Pediatr
; 59(1): 71-75, 2017.
Article
en En
| MEDLINE
| ID: mdl-29168367
Turan Ö, Anuk-Ince D, Olcay L, Sezer T, Gülleroglu K, Yilmaz-Çelik Z, Ecevit A. Neonatal cerebral sinovenous thrombosis: Two cases, two different gene polymorphisms and risk factors. Turk J Pediatr 2017; 59: 71-75. Cerebral sinovenous thrombosis (CSVT) is a rare disease in the neonatal period and also the greatest risk of neonatal mortality and morbidity. In this report, we presented two cases with CSVT and different risk factors. One of these cases had methylenetetrahydrofolate reductase (MTHFR) C677T homozygous polymorphism and the other case had both MTHFR A1298C homozygous polymorphism, plasminogen activator inhibitor-1 (PAI-1) 4G/ 5G polymorphism and elevated lipoprotein a. Early diagnosis and prompt initiation of therapy of neonatal CSVT may prevent neonatal mortality and poor long-term neurodevelopmental outcomes.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Trombosis de los Senos Intracraneales
/
Inhibidor 1 de Activador Plasminogénico
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Metilenotetrahidrofolato Reductasa (NADPH2)
Tipo de estudio:
Etiology_studies
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Risk_factors_studies
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Screening_studies
Límite:
Female
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Humans
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Male
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Newborn
Idioma:
En
Revista:
Turk J Pediatr
Año:
2017
Tipo del documento:
Article
País de afiliación:
Turquía
Pais de publicación:
Turquía