All individuals with variants in gene ALKBH8

5 entries on 1 page. Showing entries 1 - 5.
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00240154 Family 1 PubMed: Monies 2019 4-generation family, 3 affected (2 brothers/sister), unaffected heterozygous carrier parents/relatives F;M yes Saudi Arabia - - - - - ID see paper; …, intellectual disability (3/3), epilepsy (2/3), global developmental delay (3/3) 1 3 Johan den Dunnen
00240155 Family 2 PubMed: Monies 2019 5-generation family, 4 affected brothers, unaffected heterozygous carrier parents/relatives M yes Saudi Arabia - - - - - ID see paper; …, intellectual disability (4/4), epilepsy (4/4), global developmental delay (4/4) 1 4 Johan den Dunnen
00465983 FamPatIV1 PubMed: Waqas 2022, Journal: Waqas 2022 4-generation family, 1 affected, unaffected heterozygous carrier parents F - Pakistan - - - - - ? see paper; ..., developmental delay; normal pregnancy; global developmental delay; speech delay; mild–intellectual disability; seizure; hypotonia; ; weak reflexes; mild hyperactivity; no anxiety; normal sleep; no repetitive tics; no major deficiency in memory/mathematical abilities; dysmorphic features; 14y-height 146cm, weight 47kg, OFC 51,5cm; MRI brain normal; polydactyly; normal hearing; no eye anomalies; ECG normal; no muscular anomalies 1 1 Muhammad Umair
00468567 FamPatBAB13277 PubMed: Saad 2021 2-generation family, affected sister/brother, unaffected heterozygous carrier parents M - Egypt - - - - - ID see paper; ..., intellectual disability, global developmental delay 1 2 Johan den Dunnen
00468568 FamPatII2/3 PubMed: Maddirevula 2022 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F yes Yemen - - - - - ID see paper; ..., developmental delay; intellectual disability 1 2 Johan den Dunnen
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