Article
Turner syndrome in diverse populations.
American journal of medical genetics. Part A - 1 Feb 2020
Kruszka Paul, Addissie Yonit A, Tekendo-Ngongang Cedrik, Jones Kelly L, Savage Sarah K, Gupta Neerja, Sirisena Nirmala D, Dissanayake Vajira H W, Paththinige C Sampath, Aravena Teresa, Nampoothiri Sheela, Yesodharan Dhanya, Girisha Katta M, Patil Siddaramappa Jagdish, Jamuar Saumya Shekhar, Goh Jasmine Chew-Yin, Utari Agustini, Sihombing Nydia, Mishra Rupesh, Chitrakar Neer Shoba, Iriele Brenda C, Lulseged Ezana, Megarbane Andre, Uwineza Annette, Oyenusi Elizabeth Eberechi, Olopade Oluwarotimi Bolaji, Fasanmade Olufemi Adetola, Duenas-Roque Milagros M, Thong Meow-Keong, Tung Joanna Y L, Mok Gary T K, Fleischer Nicole, Rwegerera Godfrey M, de Herreros María Beatriz, Watts Johnathan, Fieggen Karen, Huckstadt Victoria, Moresco Angélica, Obregon María Gabriela, Hussen Dalia Farouk, Ashaat Neveen A, Ashaat Engy A, Chung Brian H Y, Badoe Eben, Faradz Sultana M H, El Ruby Mona O, Shotelersuk Vorasuk, Wonkam Ambroise, Ekure Ekanem Nsikak, Phadke Shubha R, Richieri-Costa Antonio, Muenke Maximilian
Abstract excerpt
Turner syndrome (TS) is a common multiple congenital anomaly syndrome resulting from complete or partial absence of the second X chromosome. In this study, we explore the phenotype of TS in diverse populations using clinical examination and facial analysis technology. Clinical data from 78 individuals and images from 108 individuals with TS from 19 different countries were analyzed. Individuals were grouped into...
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