All individuals with variants in gene PIK3R2

9 entries on 1 page. Showing entries 1 - 9.
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00034521 - - - M no Italy - - - yes - MPPH1 MPPH syndrome 1 1 Norine Voisin
00056046 - PubMed: Riviere 2012, Journal: Riviere 2012 2-generation family, 3 affected sibs (2F, M), unaffected non-carrier parents/sister; suspected germline mosaicism parent since 3 affected sibs share germline variant not detected in either parent (2 tissues) M no - European >16y - - - MPPH1 mild developmental delay particularly involving speech, later diagnosed with Asperger syndrome; 18m-third ventriculostomy for progressive ventriculomegaly (HP:0002119), no seizures; 12.5y MRI-brain striking megalencephaly (HP:0001355), bilateral perisylvian polymicrogyria (HP:0002126), borderline cerebellar tonsillar ectopia, moderately thick corpus callosum, no vascular malformations, no digital anomalies (no polydactyly (-HP:0010442), no syndactyly (-HP:0001159)) 1 3 Johan den Dunnen
00073756 - - - F no Spain - - - - - BFPP - 1 1 NeuroMeGen
00079901 - PubMed: Mirzaa 2015 - - - - - - - - - ? Diagnosis: Bilateral perisylvian polymicrogyria (BPP) 1 1 Jelena Čalyševa
00079902 - PubMed: Mirzaa 2015 - - - - - - - - - ? Diagnosis: Bilateral perisylvian polymicrogyria (BPP) 1 1 Jelena Čalyševa
00081754 - PubMed: Mirzaa 2015 - - - - - - - - - - - 1 1 Johan den Dunnen
00081755 - PubMed: Mirzaa 2015 - - - - - - - - - - - 1 1 Johan den Dunnen
00374807 S-4894 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00464536 323321 - - M no Germany - - - - - MPPH1 Intellectual disability, Macrocephaly, Seizure, Neurodevelopmental delay 1 1 Andreas Laner
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