NotCH 1 mutation in a patient with spontaneous and recurrent dissections of extracranial arteries
Author
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Guevara Oliva, Carlos
Author
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Farías Gontupil, Gonzalo
Author
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Bulatova, Kateryna
Author
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Alarcón Arias, Pablo
Author
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Soruco Pastrana, Wendy
Author
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Robles Morales, Carlos
Author
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Morales, Marcelo
Admission date
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2018-04-06T19:00:24Z
Available date
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2018-04-06T19:00:24Z
Publication date
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2017-06-09
Cita de ítem
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Frontiers in Neurology Vol 8 Article 245 (2017)
es_ES
Identifier
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10.3389/fneur.2017.00245
Identifier
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https://repositorio.uchile.cl/handle/2250/147199
Abstract
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Dissections of extracranial arteries are estimated to account for only 2% of all ischemic strokes but for approximately 20% of strokes in patients younger than 45 years old. Most dissections of extracranial arteries involve some trauma stretch, mechanical stress, or connective tissue abnormalities. In the absence of these disorders, determining the etiology of recurrent extracranial dissections is quite challenging because the underlying nature of these cases is poorly understood. We report the case of a 44-year-old female with recurrent dissections of the vertebral and carotid arteries associated with a heterozygous mutation p.Pro2122Leu in the NOTCH 1 gene. Her mother with a thoracic aortic aneurysm was also positive for this variant.