RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164070021 T1 FG Syndrome (Opitz-Kaveggia Syndrome) T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164070021 RD 2024/03/28 AB Genetically transmitted polymalformative syn­drome characterized by short stature with a disproportionately large head, imperforate anus, hypotonia, and agenesia of corpus callosum. Other clinical presentations include developmental delay, characteristic facial appearance, relative macrocephaly and anomalies affecting the genitourinary, gastrointestinal, and musculoskeletal systems. Genitourinary abnormalities are cryptorchidism, hypospadias, inguinal hernia, hydrocele, and occasional anomalies of renal or ureteral development.