TY  - CHAP
M1  - Book, Section
TI  - Michels Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164078651
ER  -