Bilateral frontal polymicrogyria: Difference between revisions
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Latest revision as of 18:24, 18 March 2025
Definition[edit]
Bilateral frontal polymicrogyria is one of the rarest subtypes of polymicrogyria. It is a symmetric and bilateral form (in both brain hemispheres) that only involves the frontal lobes without including the area located behind the Sylvius fissure or the area located behind the Rolando sulcus.
Types[edit]
Some researchers classify the condition into two different forms: bilateral frontal polymicrogyria and the bilateral frontoparietal.
Cause[edit]
The frontoparietal form is caused by changes (mutations) in the GPR56 gene but the cause for the frontal form of polymicrogyira is still not known.
Signs and symptoms[edit]
Signs and symptoms included delayed motor and language milestones; spastic (stiffness) hemiparesis (weakness in one side of the body) or quadriparesis (weakness in all four limbs of the body); and mild to moderate intellectual disability. Seizures may also be present.
Clinical presentation[edit]
For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed.
80%-99% of people have these symptoms
- Delayed speech and language development(Deficiency of speech development)
- Global developmental delay
30%-79% of people have these symptoms
- Intellectual disability, mild(Mental retardation, borderline-mild)
- Spastic tetraparesis
5%-29% of people have these symptoms
- EEG abnormality
Diagnosis[edit]
- The diagnosis of PMG is typically made by MRI since computed tomography (CT) and other imaging methods do not have high enough resolution or adequate contrast to identify the small folds that define PMG.<ref>Stutterd CA, Dobyns WB, Jansen A, et al. Polymicrogyria Overview. 2005 Apr 18 [Updated 2018 Aug 16]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2021. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1329/</ref>[1].
- In 5% of cases, PMG is detected on prenatal ultrasound examination by the presence of abnormalities – usually microcephaly and/or associated brain malformations.
Treatment[edit]
Treatment is based on the signs and symptoms present in each person.
References[edit]
<references />
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NIH genetic and rare disease info[edit]
Bilateral frontal polymicrogyria is a rare disease.
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Rare diseases - Bilateral frontal polymicrogyria
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