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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Genetic syndromes screening by facial recognition technology: VGG-16 screening model construction and evaluation

Fig. 1

Facial dysmorphism in children with genetic syndromes. Williams-Beuren syndrome (1–7). Noonan syndrome (8–15). Down syndrome (16–21). Marfan syndrome (22–26). Loeys-Dietz syndrome (27–30). Alagille syndrome (31–34). DiGeroge syndrome (35–37). Acromicric and Geleophysic dysplasia (38–40). Kabuki syndrome (41–42). Barth syndrome (43–44). Cornelia de Lange syndrome (45–46). Koolen-de Vires syndrome (47–48). 14q32 duplication syndrome (49–50). Congenital mental retardation, AD (51–52). 8p23.1 deletion syndrome (53–54). 21q22.3 deletion syndrome (55–56). Helsmoortel-Van der Aa syndrome (57). Mulibrey nanism (58). Congenital fibrosis of extraocular muscles (59). Mandibulofacial dysostosis-microcephaly syndrome (60). Cerebro-oculo-facio-skeletal syndrome (61). Oculo‐facio‐cardio‐dental syndrome (62). Wolf-Hirschhorn syndrome (63). Costello syndrome (64). Cri du Chat syndrome (65). Stickler syndrome (66). Coffin-Siris syndrome (67). Klippel-Feil syndrome (68). Congenital contractural arachnodactyly (69). 16p11.2 duplication syndrome (70). Holt-Oram syndrome (71). X-Linked Oto-palato-digital spectrum disorders (72). 16p11.2 microdeletion syndrome (73). Brittle cornea syndrome (74). 18q microdeletion syndrome (75). The grey bar is used to protect privacy

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