RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164079502
T1 Muller Barth Menger Syndrome
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=1164079502
RD 2025/05/21
AB It  is  a  genetic  disease  characterized  by  the  presence  of  multiple  cerebral  malformation,  seizures,  hypertrichosis,  distinct  face,  claw  hands,  and  overlapping  fingers.