TY - CHAP M1 - Book, Section TI - Feingold Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Polymalformative condition characterized by esophageal/duodenal atresia, limb abnormalities (hand/foot), short palpebral fissures, microcephaly and learning disabilities. It is considered similar to the ☞VACTERL Syndrome (Vertebral defects, Anal atresia, Cardiac defects, TracheoEsophageal fistula, Renal anomalies, and Limb abnormalities) with in addition microcephaly and severe learning deficiencies. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/09 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164069843 ER -