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hypertyrosinemia - translation to russian
AMINO ACID METABOLIC DISORDER THAT INVOLVES IMPAIRED BREAK DOWN OF THE AMINO ACID TYROSINE
Hereditary Tyrosinemias; Hypertyrosinemia; Tyrosinaemia; Tyrosinemia I; Tyrosinemias
hypertyrosinemia
медицина
гипертирозинемия
тирозинемия
tyrosinosis
TYROSINEMIA THAT HAS MATERIAL BASIS IN DEFICIENCY OF THE ENZYME FUMARYLACETOACETATE HYDROLASE RESULTING IN AN INCREASE IN FUMARYLACETOACETATE WHICH INHIBITS PREVIOUS STEPS IN TYROSINE DEGRADATION LEADING TO AN ACCUMULATION OF TYROSINE IN THE BODY
Type I tyrosinemia; Hepatorenal tyrosinemia; Tyrosinemia type 1; Tyrosinosis; Draft:Tyrosinemia (Type I); Tyrosinemia (Type I)
медицина
тирозиноз
Wikipedia
Tyrosinemia
Tyrosinemia or tyrosinaemia is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Symptoms of untreated tyrosinemia include liver and kidney disturbances. Without treatment, tyrosinemia leads to liver failure. Today, tyrosinemia is increasingly detected on newborn screening tests before any symptoms appear. With early and lifelong management involving a low-protein diet, special protein formula, and sometimes medication, people with tyrosinemia develop normally, are healthy, and live normal lives.
