TY  - CHAP
M1  - Book, Section
TI  - Marinesco-Sjögren Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Very  rare  genetic  disorder  characterized  by  the  association  of  cerebellar  ataxia  with  postnatal  congenital  cataracts,  delayed  mental  and  physical  development  (spasticity),  very  small  stature,  and  hypotonia.  The  designation  “hereditary  oligophrenic  cerebellolental  degeneration"  has  been  suggested.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58075278
ER  -