A Neonate Diagnosed with Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome with Mutation
Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP) is a rare genetic disorder characterized by megalencephaly, polymicrogyria, body overgrowth, and cutaneous capillary malformations. It has been reported recently that MCAP is related to a somatic mosaic mutation in the phosphatidyl...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Korean Society of Neonatology,
2023-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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