Tyrosinemia type I is a genetic disorder that disrupts the metabolism of the amino acid tyrosine, resulting in damage primarily to the liver along with...
30 KB (3,369 words) - 09:15, 17 November 2023
catabolic pathway, and are inherited in an autosomal-recessive pattern. Type I tyrosinemia results from a mutation in the FAH gene, which encodes the enzyme...
7 KB (685 words) - 01:50, 27 February 2022
observed liver enzyme activity in FAH deficiency during hereditary tyrosinemia type 1. In humans, this enzyme is mainly expressed in the liver. FAH is...
21 KB (2,536 words) - 22:56, 3 September 2024
phenylketonuria tyrosinemia maple syrup urine disease glutaric acidemia type 1 Urea Cycle Disorder or Urea Cycle Defects Carbamoyl phosphate synthetase I deficiency...
15 KB (1,517 words) - 22:46, 6 September 2024
genetically inherited condition of copper metabolism), Lowe syndrome, tyrosinemia (type I), galactosemia, glycogen storage diseases, and hereditary fructose...
12 KB (1,203 words) - 04:58, 14 August 2024
lead poisoning and succinylacetone, whose levels are increased in tyrosinemia type I, inhibit ALAD. Therefore, these conditions should also be considered...
10 KB (972 words) - 21:09, 18 July 2024
in a child with Henoch–Schönlein purpura, or succinylacetone for Tyrosinemia Type I.[citation needed] As opposed to symptoms (reported subjectively by...
9 KB (736 words) - 22:08, 9 April 2024
dehydratase deficiency or in patients with symptoms due to hereditary tyrosinemia type I. In cases of mercury- or arsenic poisoning-induced porphyria, other...
64 KB (6,621 words) - 21:00, 29 August 2024
cutanea tarda, hereditary coproporphyria, variegate porphyria) and tyrosinemia type I are risk factors for hepatocellular carcinoma. The diagnosis of an...
90 KB (10,116 words) - 18:28, 6 September 2024
Liver Function and Extend Survival in a Mouse Model of Hepatorenal Tyrosinemia Type I". Advanced Materials. 30 (52): 1805308. Bibcode:2018AdM....3005308C...
19 KB (2,174 words) - 09:44, 17 August 2024