TY  - CHAP
M1  - Book, Section
TI  - Laurence Moon Syndrome (LMS)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164076410
ER  -