RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164084913
T1 Sensenbrenner 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=1164084913
RD 2024/04/25
AB Ciliopathy.  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.