A Novel Heterozygous De Novo MORC2 Missense Variant Causes an Early Onset and Severe Neurodevelopmental Disorder

Figure 1

Frontal view of patient at 51 weeks of age displaying several distinctive features including almond-shaped eyes with epicanthic folds, mild ptosis bilaterally, widened nasal bridge, mild brachydactyly in her feet, and a degree of micrognathia (Figure 1).