RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164072471 T1 Hennekam 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=1164072471 RD 2024/10/07 AB Rare, autosomal recessive medical condition that is characterized with intestinal lymphangiectasia and lymphedema of the limbs, genital, and face, dysmorphic facial appearance and severe mental retardation.