RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164069705
T1 Familial Progressive Scleroderma
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=1164069705
RD 2024/04/23
AB Disorder  characterized  by  progressive  systemic  sclerosis  (scleroderma),  calcium  deposits  (calcinosis)  usually  in  the  fingers,  Raynaud  Syndrome,  loss  of  muscle  control  of  the  esophagus  (difficult  swallowing),  osseous  deformity  of  the  fingers  (sclerodactyly),  and  small  red  spots  (telangiectasia)  on  the  skin  (fingers,  face)  or  inside  the  mouth.