Polymicrogyria Support

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PMG Awareness Organization Inc. - Unlocking the mysteries ...

    https://pmgawareness.org/
    The PMG Awareness website has been incredibly helpful for us. At the time of our daughters diagnosis, we were overwhelmed and devastated. Yet discovering this site not only helped us to educate ourselves further about Polymicrogyria, but it also opened up a whole new community of support …

Polymicrogyria - Genetics Home Reference - NIH

    https://ghr.nlm.nih.gov/condition/polymicrogyria
    Oct 29, 2019 · Polymicrogyria is a condition characterized by abnormal development of the brain before birth. The surface of the brain normally has many ridges or folds, called gyri. In people with polymicrogyria, the brain develops too many folds, and the folds are unusually small.The name of this condition literally means too many (poly-) small (micro-) folds (-gyria) in the surface of the brain.

Polymicrogyria Genetic and Rare Diseases Information ...

    https://rarediseases.info.nih.gov/diseases/12271/polymicrogyria
    Oct 12, 2015 · Polymicrogyria is a condition characterized by abnormal development of the brain before birth. Specifically, the surface of the brain develops too many folds which are unusually small. ... Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. ...

Polymicrogyria - Wikipedia

    https://en.wikipedia.org/wiki/Polymicrogyria
    Polymicrogyria (PMG) is a condition that affects the development of the human brain by multiple small gyri creating excessive folding of the brain leading to an abnormally thick cortex.This abnormality can affect either one region of the brain or multiple regions. The time of onset has yet to be identified; however, it has been found to occur before birth in either the earlier or later stages ...Specialty: Neurology

Bilateral perisylvian polymicrogyria Genetic and Rare ...

    https://rarediseases.info.nih.gov/diseases/6011/bilateral-perisylvian-polymicrogyria
    Nov 26, 2018 · Bilateral perisylvian polymicrogyria (BPP) is a rare neurological disorder that affects the cerebral cortex (the outer surface of the brain). BPP is a subtype of a broader condition known as polymicrogyria. The cerebral cortex of the brain normally consists of several deep folds and grooves.

Polymicrogyria Overview - GeneReviews® - NCBI Bookshelf

    https://www.ncbi.nlm.nih.gov/books/NBK1329/
    Apr 18, 2005 · Although polymicrogyria in all its forms collectively is a fairly common brain malformation, each individual disorder in which it can be observed is rare. Perisylvian polymicrogyria is the most commonly described syndrome; its prevalence, like that of the other syndromes with polymicrogyria, remains unknown.

Congenital Bilateral Perisylvian syndrome Contact

    https://contact.org.uk/advice-and-support/medical-information/conditions/c/congenital-bilateral-perisylvian-syndrome/
    The term congenital bilateral perisylvian syndrome (CBPS) describes a structural malformation of the brain. The underlying abnormality is known as 'polymicrogyria', which is a malformation of the cerebral cortex (outer layer of the brain). ... Information and support in the UK for congenital bilateral perisylvian syndrome is provided by the ...

The Syndrome of Perisylvian Polymicrogyria with Congenital ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888893/
    Bilateral perisylvian polymicrogyria (BPP) is a syndrome characterized clinically by epilepsy, cognitive impairment, and the distinct feature of oromotor apraxia in the majority of affected cases . BPP may exist as a familial condition and appears to be genetically heterogeneous [5,6].Cited by: 12



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