Related MeSH Hierarchy (4)
Diseases [C] » Musculoskeletal Diseases [C05] » Musculoskeletal Abnormalities » Craniofacial Abnormalities » Megalencephaly » Hemimegalencephaly
Diseases [C] » Nervous System Diseases [C10] » Nervous System Malformations » Malformations of Cortical Development » Malformations of Cortical Development, Group I » Megalencephaly » Hemimegalencephaly
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Musculoskeletal Abnormalities » Craniofacial Abnormalities » Megalencephaly » Hemimegalencephaly
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Nervous System Malformations » Malformations of Cortical Development » Malformations of Cortical Development, Group I » Megalencephaly » Hemimegalencephaly
Description
Rare MALFORMATIONS OF CORTICAL DEVELOPMENT, GROUP I characterized by the enlargement of one side of the brain. It is associated with seizures, partial paralysis, and mental retardation. MeSH
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