Two cases of familial cerebral cavernous malformation caused by mutations in the gene

• Главные авторы: Im-Yong Yang (Автор), Mi-Sun Yum (Автор), Eun-Hee Kim (Автор), Hae-Won Choi (Автор), Han-Wook Yoo (Автор), Tae-Sung Ko (Автор)
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• Опубликовано: Korean Pediatric Society, 2016-06-01T00:00:00Z.
• Предметы: article
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Cerebral cavernous malformation (CCM) is a vascular malformation characterized by abnormally enlarged capillary cavities without any intervening neural tissue. We report 2 cases of familial CCMs diagnosed with the CCM1 mutation by using a genetic assay. A 5-year-old boy presented with headache, vomi...