RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164078632
T1 Meyer-Betz Disease
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=1164078632
RD 2024/04/18
AB It  is  a  rare  metabolic  disorder  characterized  by  an  idiopathic  primary  myoglobinuria.  The  two  clinical  entities  of  this  disease  are  type  I,  associated  with  an  onset  after  physical  exertion,  and  type  II,  that  occurs  after  infection.  Clinically,  the  symptoms  include  a  classical  triad  consisting  of  muscle  pain,  generalized  weakness,  and  discolored  brown  urine  as  a  result  of  the  excretion  of  myoglobin.