Two cases of familial cerebral cavernous malformation caused by mutations in the gene
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...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Korean Pediatric Society,
2016-06-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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