Supplementary Fig. 1: Main clinical features of affected individuals.
From: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
a, Craniofacial appearance of affected individuals showing hemifacial microsomia in all subjects. b, Patchy alopecia of hair and beard. c, Teeth anomalies consisting of oligodontia, microdontia, and conical teeth. d, Variable degrees of acral anomalies including symmetric or asymmetric brachydactyly, syndactyly, and polydactyly. Photograph of subject S3 was taken after surgery. e, Linear hypopigmentation following Blaschko’s lines on trunk, limbs, and face. See Supplementary Table 1 for additional details. We obtained written consent to publish photographs of these individuals.
