Due to the congenital nature of neuronal migration disorders, most patients do not recover from their symptoms. The course of disease tends to be static.
The royal family's lineage can be traced back for generations.
a diverse group of congenital brain abnormalities that arise specifically from defective formation of the central nervous system .
In lissencephaly or agyria, neuronal migration fails globally, causing the brain to appear completely smooth and have abnormal layering in the cortex.
Lissencephaly is part of a spectrum of brain malformations, which are referred to as the agyriapachygyria-band spectrum and are caused by abnormalities in neuronal migration, a critical process in brain development
Barriers to migration refer to obstacles or challenges that individuals face when trying to move from one place to another, such as legal restrictions, lack of resources, cultural differences, or physical barriers like borders or bodies of water. These barriers can make it difficult for people to relocate or seek better opportunities in other areas.
The most well characterized genes include DCX on the X chromosome, responsible for double cortex syndrome, and LIS1 on chromosome 17, the first gene identified for lissencephaly.
Depends on what you mean... but I'll try.There is migration, chain migration, forced migration, voluntary migration, net-in migration, net-out migration, immigration, emmigration, countermigration.These are Human Geographic terms by the way. That makes about 9 types of migration.
Neuronal cell body
International Organization for Migration
Diagnosis is usually made by neuroimaging. CT scan or MRI of the brain will show the characteristic abnormality. MRI has better resolution and may detect polymicrogyria or small heterotopias more easily than CT.
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