TY  - CHAP
M1  - Book, Section
TI  - Lambert Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164076224
ER  -