RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164068518
T1 Dyskeratosis Congenita
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=1164068518
RD 2024/04/20
AB Dyskeratosis  congenita  is  a  genodermatosis  characterized  by  the  triad  of  hyperpigmentation  of  the  skin,  dystrophy  of  the  nails,  leukoplakia  of  mucous  membranes,  and  in  addition  the  presence  of  progressive  pancytopenia.  It  has  a  highly  variable  phenotype.