tyrosinosis - перевод на арабский
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tyrosinosis - перевод на арабский


tyrosinosis         
  • Tyrosinemia type I has an autosomal recessive pattern of inheritance
  • Pathophysiology of metabolic disorders of tyrosine, resulting in elevated levels of tyrosine in blood.
  • Nitisinone
  • Tyrosine metabolic pathway. Fumarylacetoacetate hydrolase (FAH) is shown to be nonfunctional, leading to the accumulation of maleylacetoacetate (MAA) and succinylacetoacetate (SAA), the later of which is converted to succinylacetone (SA).
  • Tyrosine
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)
‎ الدَّاءُ التِّيروزينيّ‎
tyrosinosis         
  • Tyrosinemia type I has an autosomal recessive pattern of inheritance
  • Pathophysiology of metabolic disorders of tyrosine, resulting in elevated levels of tyrosine in blood.
  • Nitisinone
  • Tyrosine metabolic pathway. Fumarylacetoacetate hydrolase (FAH) is shown to be nonfunctional, leading to the accumulation of maleylacetoacetate (MAA) and succinylacetoacetate (SAA), the later of which is converted to succinylacetone (SA).
  • Tyrosine
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)
الدَّاءُ التِّيروزينيّ