RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58075304
T1 Maroteaux Cohen-Solal Bonaventure Syndrome
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=58075304
RD 2024/04/19
AB Severe  congenital  genetic  disease  characterized  by  undermineralization  of  skull  and  bones,  thin  ribs,  thoracic  collapse,  multiple  fractures,  short  stature,  and  prenatal  onset.  It  is  not  believed  to  be  linked  to  collagen  metabolism  defects.  Facies  is  peculiar.