617768.1

United Arab Emirates

Motor delay; Global developmental delay; Abnormal facial shape

Female

Yes

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_170606.3:c.9391C>T	1	NA	Kleefstra Syndrome 2
NM_020988.3:c.680C>T	1	NA	Neurodevelopmental Disorder with Involuntary Movements