RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164069650
T1 Familial Osteodysplasia
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164069650
RD 2024/04/19
AB Inherited  disorder  believed  to  be  an  autosomal  recessive  trait.  It  is  characterized  by  midface  hypoplasia,  malformation  of  the  mandible,  hypoplastic  zygomatic  bones,  and  abnormally  pointed  chin.