Fig.1From: New pathogenic variants of ALMS1 gene in two Chinese families with Alström SyndromeFundus and body skin examination of the family 1 with Alström Syndrome. a, b Fundus photography of the individuals from II:1 showing nothing changed. c, d Optical Coherence tomography (OCT): showing standard foveal architecture in the II:1. e, f Fundus Autofluorescence (FAF): showing normal in the II:1. g, h Skin photography of the elbow and knee joint: showing acanthosis nigricansBack to article page