TY  - CHAP
M1  - Book, Section
TI  - Mohr-Tranebjaerg Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Novel  rare  genetic  type  of  mitochondrial  disease.  Progressive  deafness  becomes  evident  at  age  3  to  5  years.  Severe  dysarthria  and  occasional  bizarre  posturing  of  head  and  neck  are  possible.  Dystonia,  spasticity,  dysphagia  and  optic  atrophy  appear  in  adult  life.  Patients  are  prone  to  seizures  and  lactate  acidosis.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58076411
ER  -