TY  - CHAP
M1  - Book, Section
TI  - Meretoja Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - It  is  a  primary  hereditary  systemic  amyloidosis  (Type  II)  characterized  by  cardiac  and  airway  implications.  Clinical  features  include  corneal  lattice  dystrophy  and  cranial  neuropathy  (eg,  facial  paresis),  nephrotic  syndrome  and  renal  failure,  and  cutis  laxa.  Progressive  peripheral  polyneuropathy  is  mainly  affecting  vibration  and  touch  senses  is  a  feature  present  in  these  individuals.  The  onset  of  the  disease  begins  much  later  in  life  usually  around  the  age  of  50  to  70  years.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/17
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164078396
ER  -