All individuals with variants in gene AP2M1

4 entries on 1 page. Showing entries 1 - 4.
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00235329 Pat1 PubMed: Helbig 2019, Journal: Helbig 2019 - F no - Europe - - - - ENC see paper; …, global developmental delay; 1y9m-onset seizures, atypical absence, myoclonic atonic, absence with eyelid myoclonia, drug-responsive; moderate intellectual disability; no autism spectrum disorder; truncal and gait ataxia; hypotonia; MRI parieto-occipital white matter abnormalities; EEG generalized polyspike-wave discharges 1 1 Johan den Dunnen
00235330 Pat2 PubMed: Helbig 2019, Journal: Helbig 2019 - F no - Europe - - - - ENC see paper; …, global developmental delay; 1y3m-onset seizures, atonic, atypical absence, absence with eyelid myoclonia, drug-resistant; moderate intellectual disability; no autism spectrum disorder, aggressive and self-harming behavior; absent ataxia; hypotonia; MRI normal; EEG 3–4 Hz generalized spike-wave discharges 1 1 Johan den Dunnen
00235331 Pat3 PubMed: Helbig 2019, Journal: Helbig 2019 - F no Mexico - - - - - ENC see paper; …, global developmental delay; 3y-onset seizures, atonic, bilateral tonic-clonic, drug-resistant; severe intellectual disability; autism spectrum disorder; gait ataxia only; hypotonia; chorea and myoclonus; prominent maxilla, thin upper lip; MRI normal; EEG generalized spike-wave discharges 1 1 Johan den Dunnen
00235332 Pat4 PubMed: Helbig 2019, Journal: Helbig 2019 - F no Germany;United Kingdom (Great Britain) Jewish - - - - ENC see paper; …, global developmental delay; 4y-onset seizures, focal impaired-awareness seizures, partially drug-responsive; severe intellectual disability; autism spectrum disorder; truncal and gait ataxia; hypotonia; tremor; long, thin hands and feet; MRI normal; EEG multifocal epileptiform activity 1 1 Johan den Dunnen
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