RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164060321
T1 Acrocephalosyndactyly Type I: Apert Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164060321
RD 2024/04/25
AB Agenesis  or  premature  closure  of  the  cranial  sutures,  midface  hypoplasia,  and  symmetrical  syndactyly  of  hands  and  feet  involving  at  least  the  second,  third,  and  fourth  digits.  Partial  cervical  spinal  fusion  is  common.  Numerous  facial  anomalies  are  seen.  Heart  defects  may  be  present.