RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164077737
T1 Marden-Walker 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=1164077737
RD 2020/07/04
AB It  is  a  very  rare  inherited  connective  tissue  disorder  that  is  characterized  by  in  75%  of  affected  children,  blepharophimosis,  a  small  mouth,  micrognathia,  kyphoscoliosis,  radioulnar  synostosis,  and  multiple  joint  contractures.  Other  clinical  features  include  microcytic  dysplastic  kidneys,  dextrocardia,  Dandy-Walker  malformation,  agenesis  of  the  corpus  callosum,  arachnodactyly,  camptodactyly,  cleft  lip/palate  or  a  high-arched  palate,  growth  delay,  and  slow  muscle  movement.