RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164088050
T1 Weyers Syndrome II
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=1164088050
RD 2024/04/16
AB This  is  a  medical  condition  with  an  onset  of  symptoms  at  birth,  affecting  both  sexes,  and  characterized  by  postaxial  polydactyly  of  the  hands  and  feet,  hexadactyly  and  fusion  of  fifth  and  sixth  metatarsals  and  metacarpals,  as  well  as  bony  clefts  of  the  mandibular  symphysis.  Other  features  include  orodental  anomalies,  hypoplastic  and  dysplastic  nails,  short  stature,  micrognathia,  small  mouth,  and  hypoplasia  of  the  larynx.  Congenital  heart  defect  may  be  present.