RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164076224
T1 Lambert Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164076224
RD 2024/04/25
AB It  is  a  very  rare  inherited  polymalformative  syndrome  characterized  by  the  association  between  branchial  arch  dysplasia  (malar  hypoplasia,  macrostomia,  periauricular  tags,  meatal  atresia,  and  clubfeet,  inguinal  hernia,  and  intrahepatic  biliary  atresia).  Mental  retardation  is  present.