Duplication 2p16 is associated with perisylvian polymicrogyria
Dina Amrom1,2,3, Annapurna Poduri4,5, Jennifer S Goldman6
1Neurogenetics Unit, Montreal Neurological Institute and Hospital, Montreal, Quebec, Canada.
American Journal of Medical Genetics. Part A
|October 30, 2019
Summary
Researchers identified a novel genetic locus for polymicrogyria (PMG), a brain malformation, on chromosome 2p16.1-p16.3. This discovery aids in understanding the genetic causes of PMG and related neurodevelopmental issues.
Area of Science:
- Neuroscience
- Genetics
- Developmental Biology
Background:
- Polymicrogyria (PMG) is a complex brain malformation with diverse causes, including genetic factors that are often challenging to pinpoint.
- Identifying specific genetic loci is crucial for understanding PMG's etiology and developing targeted interventions.
Keywords:
chromosome 2duplication 2p16.1-p16.3growth retardationintellectual disabilitypolymicrogyriaMore Related Videos
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