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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.660 Musculoskeletal Abnormalities .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.536 Megalencephaly .
C05.660.207.536.500 Hemimegalencephaly .
C05.660.207.620 Microcephaly .
C10 Nervous System Diseases .
C10.500 Nervous System Malformations .
C10.500.507 Malformations of Cortical Development .
C10.500.507.400 Malformations of Cortical Development, Group I .
C10.500.507.400.249 Megalencephaly .
C10.500.507.400.249.500 Hemimegalencephaly .
C10.500.507.400.500 Microcephaly .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.207 Craniofacial Abnormalities .
C16.131.621.207.532 Megalencephaly .
C16.131.621.207.532.500 Hemimegalencephaly .
C16.131.621.207.620 Microcephaly .
C16.131.666 Nervous System Malformations .
C16.131.666.507 Malformations of Cortical Development .
C16.131.666.507.400 Malformations of Cortical Development, Group I .
C16.131.666.507.400.249 Megalencephaly .
C16.131.666.507.400.249.500 Hemimegalencephaly .
C16.131.666.507.400.500 Microcephaly .
 Synonyms & Historicals
Malformations of Cortical Development, Group I .
Abnormal Proliferation Cortical Malformations .
Cortical Malformations, Group I .
Malformations Due to Abnormal Neuronal and Glial Proliferation or Apoptosis .
Malformations Secondary to Abnormal Neuronal and Glial Proliferation or Apoptosis .
Cortical malformations secondary to abnormal neuronal and glial CELL PROLIFERATION or APOPTOSIS in NEUROGENESIS. This group includes congenital MICROCEPHALIES; MICROLISSENCEPHALIES, megalencephalies, HEMIMEGALENCEPHALIES and cortical dysplasias with balloon cells. .
Megalencephaly .
Megacephaly .
Megalocephaly .
Macrocephalies .
Megacephalies .
Megalencephalies .
Megalocephalies .
Macrocephaly .
A congenital abnormality in which the occipitofrontal circumference is greater than two standard deviations above the mean for a given age. It is associated with HYDROCEPHALUS; SUBDURAL EFFUSION; ARACHNOID CYSTS; or is part of a genetic condition (e.g., ALEXANDER DISEASE; SOTOS SYNDROME). .
Microcephaly .
Severe Congenital Microcephaly .
Congenital Microcephalies, Severe .
Congenital Microcephaly, Severe .
Microcephalies .
Microcephalies, Severe Congenital .
Microcephaly, Severe Congenital .
Microlissencephalies .
Severe Congenital Microcephalies .
Microlissencephaly .
A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.) .
Hemimegalencephaly .
Unilateral Macrocephaly .
Unilateral Megalencephaly .
Hemimegalencephalies .
Macrocephalies, Unilateral .
Macrocephaly, Unilateral .
Megalencephalies, Unilateral .
Megalencephaly, Unilateral .
Unilateral Macrocephalies .
Unilateral Megalencephalies .
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. .