RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58083690 T1 Potter Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications YR 2006 FD 2006 PB The McGraw-Hill Companies PP New York, NY SN 9780071354554 LK accessanesthesiology.mhmedical.com/content.aspx?aid=58083690 RD 2024/03/29 AB A possible genetic disorder characterized by oligohydramnios secondary to renal diseases such as bilateral renal agenesis. Other possible renal defects include obstructive uropathy, autosomal recessive polycystic kidney disease, medullary dysplastic kidney, and renal hypoplasia. Clinical features include Potter facies (i.e., flattened nose, recessed chin), pulmonary hypoplasia, skeletal anomalies, and congenital heart defects.