TY  - CHAP
M1  - Book, Section
TI  - Meyer-Betz Disease
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164078632
ER  -