Fig. 1From: Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness – a case report for dual diagnosisPhotograph and growth curve of the proband. a Photo of the proband’s back at 2 months, he is extremely thin and skeletonizing. b The proband with low birth weight grew slowly and lagged obviously behind the referent range [7]Back to article page