Malformations of Cortical Development, Group I

MeSH 搜索器

Malformations of Cortical Development, Group I

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.

推出的年份: 2015

树号: C10.500.507.400, C16.131.666.507.400

MeSH 单一 ID: D065703

进入的组:

Malformations Due to Abnormal Neuronal and Glial Proliferation or Apoptosis
Malformations Secondary to Abnormal Neuronal and Glial Proliferation or Apoptosis
Abnormal Proliferation Cortical Malformations
Cortical Malformations, Group I

早前的内容:

Cerebral Cortex/abnormalities (1995-2007)
Malformations of Cortical Development (2008-2014)

All MeSH Categories
- Diseases Category
  - Nervous System Diseases [C10]
    - Nervous System Malformations [C10.500]
      - Malformations of Cortical Development [C10.500.507]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Congenital Abnormalities [C16.131]
      - Nervous System Malformations [C16.131.666]
        
        Malformations of Cortical Development [C16.131.666.507]
        
        Malformations of Cortical Development, Group I [C16.131.666.507.400]
        
        Megalencephaly [C16.131.666.507.400.249] add_circle
        
        Microcephaly [C16.131.666.507.400.500]
        
        Tuberous Sclerosis [C16.131.666.507.400.750]
        
        Malformations of Cortical Development, Group II [C16.131.666.507.450] add_circle
        
        Malformations of Cortical Development, Group III [C16.131.666.507.500] add_circle

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MeSH 搜索器

Malformations of Cortical Development, Group I

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