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Pachygyria

DA: 403




Developmental anomaly information

Definition: Pachygyria is a congenital malformation of the cerebral hemisphere due to abnormal cell migration, disorganized cellular architecture, failure to form six layers of cortical neurons (a four-layer cortex is common), and functional problems. . It results in unusually thick convolutions of the cerebral cortex.



Developmental anomaly parent: (empty)

Topology: Human body > Head and neck > Head > Cranium > Brain

System: Human body > Nervous system > Central nervous system > Brain

Developmental anomaly category: (empty)

Case records MDB340
Links
Observed in MDB cases
Observed in combinaisons (MDB)
Observed in malformative diseases (MDB)
Associated genes in profile
Associated genes in malformative diseases
Associated chromosomal diseases
Associated signaling pathways
Associated developmental anomalies

Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :



Last modified: 2008-07-31 17:35:52 by farideh

Created: 2008-06-13 04:59:51 by jcfournet



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