Hemimegalencephaly

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.

Year introduced: 2015 (2008)

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C05.660.207.536.500, C10.500.507.400.249.500, C16.131.621.207.532.500, C16.131.666.507.400.249.500

MeSH Unique ID: D065705

Entry Terms:

• Hemimegalencephalies
• Unilateral Megalencephaly
• Megalencephalies, Unilateral
• Megalencephaly, Unilateral
• Unilateral Megalencephalies
• Unilateral Macrocephaly
• Macrocephalies, Unilateral
• Macrocephaly, Unilateral
• Unilateral Macrocephalies

All MeSH Categories
Diseases Category
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Megalencephaly
Hemimegalencephaly

All MeSH Categories
Diseases Category
Nervous System Diseases
Nervous System Malformations
Malformations of Cortical Development
Malformations of Cortical Development, Group I
Megalencephaly
Hemimegalencephaly

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Megalencephaly
Hemimegalencephaly

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Malformations of Cortical Development
Malformations of Cortical Development, Group I
Megalencephaly
Hemimegalencephaly