RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58080105
T1 Homocystinuria (HCU)
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=58080105
RD 2024/04/18
AB Genetically  transmitted  error  of  metabolism  of  the  amino  acid  methionine  characterized  by  severe  myopia,  Marfan-like  stature  with  pectus  excavatum,  slight  mental  retardation,  and  tendency  to  develop  spontaneous,  generalized  arterial,  and  venous  thromboses  under  stress.