RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164066575 T1 Congenital Myopathy with Fiber-Type Disproportion 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=1164066575 RD 2024/10/11 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.