RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164078651
T1 Michels 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=1164078651
RD 2024/04/23
AB It  is  clinically  defined  as  a  triad  of  symptoms  that  include  blepharophimosis,  craniosynostosis,  and  epicanthus  inversus.  Other  features  include  highly  arched  eyebrows,  and  hypertelorism.  Occasional  presence  of  spinal  bifida  occulta,  cranial  asymmetry,  occipital  bone  flattening,  and  cleft  lip/palate.  Patient  may  manifest  psychological  development  delays.