RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58076629
T1 Mowat-Wilson Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58076629
RD 2024/04/23
AB Autosomal  dominant  complex  developmental  disorder  characterized  by  short  stature,  microcephaly,  severe  mental  retardation,  delayed  motor  development,  epilepsy,  and  a  wide  spectrum  of  clinically  heterogeneous  features  suggestive  of  neurocristopathies  at  the  cephalic,  cardiac,  and  vagal  nerve  levels.