RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58075847
T1 Meretoja Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58075847
RD 2024/04/20
AB Primary  hereditary  systemic  amyloidosis  (type  V)  characterized  by  cardiac  and  airway  implications.  Clinical  features  include  corneal  lattice  dystrophy  and  cranial  neuropathy  (e.g.,  facial  paresis),  nephrotic  syndrome  and  renal  failure,  and  cutis  laxa.  Peripheral  polyneuropathy  mainly  affecting  vibration  and  touch  senses  may  be  present  in  these  individuals.