RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164078165
T1 Meier-Gorlin Syndrome
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=1164078165
RD 2024/04/23
AB It  is  an  inherited  disorder  characterized  by  short  stature,  craniofacial  anomalies,  bilateral  microtia,  and  absence  of  patellae.  Other  clinical  features  include  microstomia,  microcephaly,  hypoplasia  of  the  maxillary,  and  micrognathia.  The  skeletal  anomalies  include  complete  dislocation  of  the  elbow,  hooked  clavicle,  and  clinodactyly.