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 2024/04/19
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.