RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164086685
T1 Tricho-Rhino-Phalangeal Dysplasia Type III
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=1164086685
RD 2024/04/20
AB An  extremely  rare  inherited  multisystem  disorder  characterized  by  fine,  thin  light-colored  hair,  unusual  facial  features,  abnormalities  of  the  fingers  and/or  toes,  and  multiple  abnormalities  of  epiphyses  leading  to  skeletal  dysplasia.  The  skeletal  dysplasia  is  mostly  observed  in  the  hands  and  feet.  There  are  no  exostoses.  Normal  intelligence.  Severe  end  of  TRPS  spectrum.