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Egyptian Journal of Medical Human Genetics
Fig. 1 | Egyptian Journal of Medical Human Genetics

Fig. 1

From: Co-segregation of variant NSUN2 Lue198Arg among Iranian family with intellectual disability: a case report

Fig. 1

a Pedigree of the family. The family members with ID phenotype are shown at Pedigree (in black) with segregation of the p.(Lue198Arg) variant in the NSUN2 gene. Squares represent males; circles stand for females; ± , heterozygote for p.(Lue198Arg) variant; -/- homozygous for p.(Lue198Arg) variant. Clinical features of the individual V-6 showing ptosis, broad nasal bridge, and long face. b–d Photographs of individual 4–6

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