Figure 3. Clinical phenotype of the Weill-Marchesani syndrome family. Clinical phenotype of family QT401 with Weill-Marchesani syndrome (A) ectopia lentis in QT401 II:1; (B) normal finger in QT401II3 and brachydactyly in QT401I:1, I:2, II:1, and II:2; (C) microspherophakia in QT401 II:1 and II:2 as shown by anterior segment optical coherence tomography; (D) short stature in QT401 II:1.