File:PMC4444161 mgg30003-0197-f1.png

License

Attribution 4.0 International (CC BY 4.0)

Summary

Author:Pérez-Coria M, Lugo-Trampe JJ, Zamudio-Osuna M, Rodríguez-Sánchez IP, Lugo-Trampe A, de la Fuente-Cortez B, Campos-Acevedo LD, Martínez-de-Villarreal LE,Departamento de Genética, Facultad de Medicina y Hospital Universitario "José E. González", Universidad Autónoma de Nuevo León Monterey (Openi/National Library of Medicine Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4444161_mgg30003-0197-f1&query=Aarskog%E2%80%93Scott%20syndrome&it=xg&req=4&npos=1 Description:fig01: Patients with clinical features of Aarskog syndrome. (A) Patient 1; note distinctive facial characteristics and interdigital tracts in both hands. (B) Patient 2; discrete facial features and the shawl scrotum can be appreciated. (C) Patient 3 and his mother (patient 8); note prominent forehead, widow's peak, hypertelorism, and fold under the lower lip. (D) Patient 4 with widow's peak, midface hypoplasia, ptosis, clinodactyly, and brachydactyly. (E) Patient 5, brother of patient 4, with distinctive facial features, clinodactyly, and brachydactyly.