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Bilateral frontoparietal polymicrogyria
Other Names for this Disease
- Cerebellar ataxia with neuronal migration defect
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frontal and parietal lobes and occurs in both sides of the brain (bilateral). Signs and symptoms of BFPP typically include moderate to severe intellectual disability, motor developmental delay, seizures, cerebellar ataxia, strabismus, dysconjugate gaze (eyes that are not aligned) and other findings. Some cases of BFPP are caused by mutations in the GPR56 gene, and it is inherited in an autosomal recessive manner.Bilateral frontoparietal polymicrogyria (BFPP) is an abnormality of the developing brain in which the brain develops too many folds (which are also unusually small). BFPP specifically affects the
Last updated: 8/24/2011
- Cassandra L. Kniffin. POLYMICROGYRIA, BILATERAL FRONTOPARIETAL. OMIM. March 27, 2006; http://omim.org/entry/606854. Accessed 8/24/2011.
- Genetics Home Reference (GHR) contains information on Bilateral frontoparietal polymicrogyria. This website is maintained by the National Library of Medicine.
In Depth Information
- The Online Mendelian Inheritance in Man (OMIM) is an catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Bilateral frontoparietal polymicrogyria. Click on the link to view a sample search on this topic.