RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164076410
T1 Laurence Moon Syndrome (LMS)
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164076410
RD 2022/08/12
AB This  is  a  genetic  disorder  characterized  by  retinitis  pigmentosa  (pigmentary  degeneration  of  retina  and  rod  cone  dystrophy),  ophthalmoplegia,  spastic  paraplegia,  mental  retardation,  and  cardiomyopathy.  Other  features  include  obesity,  deafness,  cataract,  polydactyly,  and  renal  insufficiency.