“…Recently, fetal growth of liver and kidneys has been shown to be impaired in intrauterine growth-retarded infants, thus supporting the concept that fetal environmentally caused "programming" may increase the risk of functional defects and diseases in later life. 4 However, no morphologic markers of impaired fetal growth that persist later in life are known to date, with the possible exceptions of fingerprints pattern abnormalities and shape of the palm 5 or a high second-to-fourthdigit finger-length ratio 6,7 in specific SGA subsets. Here, we describe a series of children with idiopathic IUGR/ SGA showing previously unrecognized, phenotypical features, including auricle shape variations, bilaterally reduced or absent hemodynamic responses of the posterior communicating arteries (PCoAs) of the circle of Willis, joint hypermobility, soft skin, and bilateral subclinical cochlear dysfunction.…”