TY  - CHAP
M1  - Book, Section
TI  - FG Syndrome (Opitz-Kaveggia Syndrome)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Genetically  transmitted  polymalformative  syn­drome  characterized  by  short  stature  with  a  disproportionately  large  head,  imperforate  anus,  hypotonia,  and  agenesia  of  corpus  callosum.  Other  clinical  presentations  include  developmental  delay,  characteristic  facial  appearance,  relative  macrocephaly  and  anomalies  affecting  the  genitourinary,  gastrointestinal,  and  musculoskeletal  systems.  Genitourinary  abnormalities  are  cryptorchidism,  hypospadias,  inguinal  hernia,  hydrocele,  and  occasional  anomalies  of  renal  or  ureteral  development.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164070021
ER  -