TY - CHAP M1 - Book, Section TI - Congenital Myopathy with Fiber-Type Disproportion A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A rare genetic myopathy presenting at birth with hypotonia and muscle weakness. Findings occurring later in life include short stature, progressive scoliosis, hip dislocation, and deformities of the feet. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/06 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164066575 ER -