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Related to tyrosinemia: tyrosinemia type 2
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  • noun

Words related to tyrosinemia

autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation

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With a portfolio of products for the treatment of Phenylketonuria, Gaucher Disease, Niemann Pick Type C, Hereditary Tyrosinemia Type 1, Urea Cycle Disorders and others, Dipharma SA works to provide solutions for people affected by inborn metabolic diseases at an affordable cost and with a global reach.
Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs.
Hereditary Tyrosinemia Type 1 (TT1) is an autosomal recessive disorder that is characterized by the deficiency of the FAH enzyme in the tyrosine catabolic pathway, resulting in the elevation of tyrosine and its byproducts in the blood, CSF, and tissues.
Tyrosinemia type I-Diagnostic issues and prenatal diagnosis.
Long-term therapy with NTBC and tyrosine-restricted diet in a murine model of hereditary tyrosinemia type I.
23] having noted that nitisinone (used in the treatment of hereditary tyrosinemia type 1) caused an increase in serum tyrosine levels, treated OCA1B mice with the drug and noted an improvement in pigmentation of the mice.
Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.
Arabs of the North also had a large portion of PPA (11/14), IVA (8/10), tyrosinemia type-1 (6/7), classical homocystinuria (2/3), and GA-II (4/8).
Hepatorenal tyrosinemia (HRT) is an autosomal recessive inborn error of metabolism which mainly affects the liver and kidneys.
Zaid has been diagnosed with Tyrosinemia type I with liver cirrhosis and improved renal fanconi syndrome with rickets.
A medical report of SQU Hospital doctors says the child has been diagnosed with Tyrosinemia type I with liver cirrhosis and improved renal fanconi syndrome with rickets.
The deprived rat lesions could not be explained by pressure, disk rotation, water immersion, infection, necrotizing vasculitis, tyrosinemia, protein deficiency, or reduced rates of mitosis.
KEY WORDS: cancer, dichloroacetate, glutathione transferase zeta, hereditary tyrosinemia, maleylacetoacetate isomerase, mitochondrial disease, peripheral neuropathy, pyruvate dehydrogenase, toxicogenetics.
He had gotten to a point where he wouldn't eat meat, and one of the effects of tyrosinemia is it turns the proteins we get from meat toxic and makes him feel bad.
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