TY  - CHAP
M1  - Book, Section
TI  - Familial Hyperlysinemia
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - The  enzyme  deficiencies  of  α-aminoadipic  semialdehyde  dehydrogenase  and  the  saccharopine  dehydrogenases  have  been  associated  with  increased  serum  levels  of  l-lysine.  The  clinical  presentation  is  very  variable  and  may  include  developmental  delay,  hypotonia,  lethargy  recurrent  emesis,  and  diarrhea.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58070458
ER  -