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... > Nervous System Diseases > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group I > Megalencephaly > Hemimegalencephaly
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group I > Megalencephaly > Hemimegalencephaly
Musculoskeletal Diseases > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Megalencephaly > Hemimegalencephaly
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Megalencephaly > Hemimegalencephaly

Preferred term

Hemimegalencephaly  

Type

  • Topical Descriptor

Broader concept

Entry terms

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

Scope note

  • 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.

History note

  • 2015 (2008); use MALFORMATIONS OF CORTICAL DEVELOPMENT 2008-2014

In other languages

URI

http://www.yso.fi/onto/mesh/D065705

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