RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58084840
T1 Rabson-Mendenhall 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=58084840
RD 2024/04/24
AB An  extremely  rare  genetic  disorder  characterized  by  severe  insulin  resistance  and  craniofacial  anomalies,  abnormalities  of  the  teeth  and  nails,  and  acanthosis  nigricans  (hyperpigmentation  and  hyperkeratosis),  particularly  of  the  neck,  groin,  and  underarms.