RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58079962
T1 HHH 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=58079962
RD 2024/04/25
AB HHH  is  an  acronym  for  hyperornithinemia-hyperammonemia-homocitrullinuria.  It  is  a  genetically  transmitted  inborn  error  of  metabolism  caused  by  a  defect  in  the  transport  of  ornithine  into  the  mitochondrial  matrix  characterized  clinically  by  early  growth  retardation,  learning  disabilities,  periodic  confusion,  and  ataxia.