TY - CHAP M1 - Book, Section TI - Hemolytic Anemia, Congenital, with Emphysema and Cutis Laxa A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Cutis laxa is an acquired or inherited skin disorder characterized by wrinkled, inelastic skin. It is a very rare syndrome that is characterized by hemolytic anemia with early-onset emphysema and cutis laxa. The presence of excessive skinfolds and loose, redundant skin leads to early diagnosis. Associated features include cardiac valve anomalies and hernias. Aortic root dilatation might result in life-threatening aortic dissection. Poor prognosis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164072374 ER -