RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164084497
T1 Schinzel Acrocallosal 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=1164084497
RD 2024/04/16
AB A  very  rare,  autosomal  recessive,  complex,  polymalformative  disease  characterized  by  corpus  callosum  agenesis  or  hypoplasia,  craniofacial  dysmorphism,  duplication  of  the  hallux,  postaxial  polydactyly,  and  severe  mental  retardation.