RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58086590
T1 Sensenbrenner Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58086590
RD 2024/04/19
AB An  autosomal  recessive  disorder  characterized  by  dolichocephaly,  sagittal  suture  synostosis,  sparse  and  slow-growing  fine  hair,  hypertelorism,  nystagmus,  taurodontia,  dental  fusion,  anteverted  nares,  brachydactyly,  clinodactyly,  narrow  thorax  leading  to  respiratory  problems,  and  mild  mental  retardation.