Figure 1From: Systemic vascular phenotypes of Loeys-Dietz syndrome in a child carrying a de novo R381P mutation in TGFBR2: a case reportDysmorphic features of the present case. The patient shows the typical facial appearance for Loeys-Dietz syndrome with ocular hypertelorism and mild strabismus (A). Other symptoms include ectopic hair growth on the right mandible (B), high-arched cleft palate with bifid uvula (C), bilateral clubfoot (D), and kyphoscoliosis (E, F).Back to article page