G20210A mutation and cerebral venous infarct: a rare presentation in a child
| Autor: | Oneza Ahmareen, Elaine Neary, Farhana Sharif |
|---|---|
| Rok vydání: | 2015 |
| Předmět: |
Advanced and Specialized Nursing
Pathology medicine.medical_specialty Cerebrum business.industry Rehabilitation medicine.disease Thrombosis Sensory Systems Speech and Hearing Psychiatry and Mental health medicine.anatomical_structure Mutation (genetic algorithm) medicine Geriatrics and Gerontology Presentation (obstetrics) business |
| Zdroj: | International Journal on Disability and Human Development. 14 |
| ISSN: | 2191-0367 2191-1231 |
| Popis: | A 14-month old male was admitted with a 1-day history of lethargy, vomiting, drowsiness, and pallor. His examination was unremarkable. Within 24 h of admission, he developed partial seizures on the right side of his face. Magnetic resonance imaging scan showed cerebral venous thrombosis. Subsequent investigations included a thrombophilia screen, which revealed the heterozygote for prothrombin mutation |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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