RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58070648
T1 Familial Progressive Scleroderma
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=58070648
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.