RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164076545 T1 Leiner 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=1164076545 RD 2024/10/08 AB It is a severe skin disorder characterized by erythroderma with an onset during infancy. The presence of seborrheic dermatitis, diarrhea, and recurrent systemic infections defines this medical condition. Other features include large patches of red skin, and delayed central nervous system development due to complement C5 deficiency (acquired deficiency in most patients).