TY  - CHAP
M1  - Book, Section
TI  - Hereditary Sensory and Autonomic Neuropathy Type I (HSAN I)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Genetic  neurodegenerative  disorder  characterized  by  a  loss  of  sensations,  especially  in  the  lower  extremities,  leading  to  perforating  skin  ulceration  and  bone  destruction  as  a  result  of  abnormal  functioning  of  the  autonomic  nervous  system.  Type  I  is  the  most  common  form  among  the  five  types  of  HSAN.  The  disease  usually  starts  during  early  adolescence  or  adulthood.  The  disease  is  characterized  by  the  loss  of  pain  sensation  mainly  in  the  distal  parts  of  the  lower  limbs  such  as  feet  and  lower  legs.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164072658
ER  -