TY  - CHAP
M1  - Book, Section
TI  - Simpson-Golabi-Behmel Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - A  rare  entity  characterized  by  prenatal  and  postnatal  overgrowth  syndrome.  Clinical  features  include  abnormal  sacrum,  absent  nails/claws,  cleft  palate  most  often  associated  with  a  cleft  of  the  lower  lip,  coarse  facial  features,  macroglossia,  coloboma,  congenital  heart  defects  (ventricular  septal  defect,  atrial  septal  defect),  diaphragmatic  hernia,  hepatomegaly,  fusion  of  cervical  vertebra  and  limited  extension,  hydronephrosis,  intestinal  malrotation,  kidney  failure,  macrocephaly,  and  increased  risk  of  embryonal  cancers.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58086910
ER  -