1.
SQUMJ-Sultan Qaboos University Medical Journal. 2015; 15 (4): 508-509
en Inglés
| IMEMR
| ID: emr-173892
2.
Anaesthesia, Pain and Intensive Care. 2015; 19 (2): 173-180
en Inglés
| IMEMR
| ID: emr-166452
RESUMEN
Glutaric aciduria type-1 [GA-1] is an autosomal recessive metabolic disorder due to the deficiency of the enzyme glutaryl-CoA dehydrogenase. The enzymatic defect leads to secondary damage to the central nervous system due to the accumulation of glutaric acid. Progressive neurologic effects with spasticity and orthopedic deformities necessitate frequent surgical and anesthetic care. We present a 13-year-old girl with glutaric academia type-1 who required anesthetic care for posterior spinal fusion. Previous reports of anesthetic care for these patients are reviewed, the end-organ involvement discussed, and options for anesthetic care presented
Asunto(s)
Femenino , Humanos , Adolescente , Encefalopatías Metabólicas , Glutaril-CoA Deshidrogenasa/deficiencia , Atención Perioperativa
3.
EMHJ-Eastern Mediterranean Health Journal. 2004; 10 (4-5): 680-684
en Inglés
| IMEMR
| ID: emr-158338