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Polymicrogyria, focal

DA: 525

Developmental anomaly information

Definition: Polymicrogyria (PMG) is a developmental malformation of the human brain characterized by an excessive number of small convolutions (gyri) on the surface of the brain. Either the whole surface or parts of the surface can be affected


  • PMG

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: Malformation

Case records MDB181, MDB369, MDB329, MDB14, MDB118, MDB329, MDB451
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: 2008-12-15 15:56:36 by farideh

Created: 2008-08-07 23:43:47 by farideh

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