Carbamoyl-phosphate synthetase 1 deficiency

Carbamoyl-phosphate synthetase 1 deficiency (CPS1D) is a rare and severe disorder of urea cycle metabolism most commonly characterized by either a neonatal-onset of severe hyperammonemia that occurs few days after birth and manifests with lethargy, vomiting, hypothermia, seizures, coma and death or a presentation outside the newborn period at any age with (sometimes) milder symptoms of hyperammonemia.

Encephalopathy

Encephalopathy is a term that means brain disease, damage, or malfunction. In general, encephalopathy is manifested by an altered mental state.


Total: 1

                      


(per page)
PMID (PMCID)
20004862
(3758690)
MIXED_SAMPLE Young Adult
Diffusion tensor imaging in arginase deficiency reveals damage to corticospinal tracts.
Oldham MS, VanMeter JW, Shattuck KF, Cederbaum SD, Gropman AL.
Pediatr Neurol. 2010;42(1):49-52.
Individuals with a proximal urea cycle disorder, such as carbamoyl phosphate synthetase deficiency 1 or ornithine transcarbamylase deficiency, may present with encephalopathy resulting from hyperammonemia.