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Published byEdwin Bradley Modified over 5 years ago
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Photographs of individuals from different families with Noonan syndrome.
Photographs of individuals from different families with Noonan syndrome. Note typical facial features with downslanting palpebral fissures (US-1.1, Br-6.1), hypertelorism (Br-1.1, Br-3.1, Br-4.5) and ptosis (Br-4.1) and short/webbed neck (Br-2.1, Po-1.1). In SOS2 patients there is marked ectodermal involvement (most pronounced in Br-2.1). Guilherme Lopes Yamamoto et al. J Med Genet 2015;52: ©2015 by BMJ Publishing Group Ltd
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