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Tyrosinemia


Tyrosinemia is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Symptoms include liver and kidney disturbances and mental retardation.
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Treatment of tyrosinemia type I includes a diet restricted in tyrosine and ... Infants and children with tyrosinemia should have regular follow-up appointments ...
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What happens when tyrosinemia 1 is treated? ... Can other members of the family have tyrosinemia 1 or be carriers? ... Does tyrosinemia 1 happen more often in ...
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The term tyrosinemia was first given to a clinical entity based on observations ... Tyrosinemia ... biochemical basis for tyrosinemia I remained enigmatic ...
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Online Medical Dictionary and glossary with medical definitions ... Tyrosinemia type I is inherited as an autosomal recessive disorder and causes ...
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tyrosinemia ( ′tirə′sēmēə ) ( medicine ) An inborn metabolic disorder in which there is a deficiency of the enzyme p -hydroxyphenylpyruvic acid
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tyrosinemia is caused by deficiency of the enzyme fumarylacetoacetate. hydrolase (FAH). Type II (oculocutaneous tyrosinemia, also known. as Richner ...
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There are 2 clinically recognized types of tyrosinemia. ... Type II (oculocutaneous tyrosinemia, also known as Richner-Hanhart syndrome; ...
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Tyrosinemia is a hereditary inborn error of metabolism that causes severe liver ... The gene defect for Tyrosinemia is an autosomal recessive genetic trait and is ...
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Important It is possible that the main title of the report Tyrosinemia, Hereditary is not the name you expected. Please check the synonyms listing to find the ...
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Tyrosinemia information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
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Hepatorenal tyrosinemia information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
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Tyrosinemia. Definition ... There is variability in age of onset, depending on the type of tyrosinemia. ... newborn screening for tyrosinemia type I is ...
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Transplantation also "cures" tyrosinemia as donor enzyme is normal ... tyrosinemia is described who developed metabolic and clinical changes compatible ...
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Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by ... Tyrosinemia is caused by the shortage (deficiency) of one of the enzymes ...
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Untreated tyrosinemia type I usually presents either in young infants with ... Tyrosinemia type I is inherited in an autosomal recessive manner. ...
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Article describes tyrosinemia type I, its symptoms, diagnosis, and treatment. ... Tyrosinemia is an inherited disorder of chromosome 15 which affects males and ...
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