TY - CHAP M1 - Book, Section TI - Hennekam Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/07 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164072471 ER -