TY - CHAP M1 - Book, Section TI - Ullrich Disease A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A very rare autosomal recessive disorder, characterized by muscular weakness, multiple contractures, and orthopedic signs noted at birth or in early infancy. Cellular immunity can be involved. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/10 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164087099 ER -