RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58077050
T1 Myoadenylate Deaminase Deficiency
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58077050
RD 2024/04/19
AB Inherited  or  secondarily  acquired  disorder  of  muscle  purine  nucleotide  metabolism.  The  clinical  manifestations  include  exercise-induced  myopathy,  postexertional  muscle  weakness  or  cramping,  prolonged  fatigue  after  exertion,  and  limping  infant  caused  by  benign  congenital  hypotonia.  Generalized  muscle  pair  is  often  manifested.