RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58076411
T1 Mohr-Tranebjaerg 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=58076411
RD 2024/04/19
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.