What does TYR stand for?

Tyrosinemia (types I, II and III)

This definition appears very rarely and is found in the following Acronym Finder categories:

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Tian Yu Plastic Packing Type Unit Report Take Young People Seriously (Almonte, Ontario, Canada) Town Youth Participation Strategies Ten Year Review (various organizations) The Young Riders (TV show) Tyler, TX, USA - Pounds Field (Airport Code) Tyrolean Airways Austria (ICAO code) Tyrosinase Tyrosine (Amino Acid)		Texas Youth Rugby Association Trans Youth Resource and Advocacy (Chicago, IL) Typhoon Tracking Tai-Yang Research Company (Knoxville, TN) Tom Yancer Race Cars (Chandler, AZ) Trace Your Route Everywhere (global positioning satellite receivers software) Tennessee Young Republican Federation Tyrosinase-Like (protein) Tyrosyl-Trna Synthetase (gene) Tokyo Young Researchers Workshop

Samples in periodicals archive:

A number of studies suggest DCA-induced liver cancer may be linked to its effects on GST-[xi], which is part of the tyrosine catabolism pathway whose disruption in type 1 hereditary tyrosinemia has been linked to increased liver cancer risk in humans.

Key issues in the modes of action and effects of trichloroethylene ...

Tyrosinemia is a genetic inborn error of metabolism, involving the amino acid tyrosine and is associated with a lack of the enzyme Fumarylacetoacetate Hydrolase (FAH).

Dietary therapies for medical disorders: finding a way to make them ...

The majority, however, are obscure diseases such as Landau Kleffner Syndrome, Wilson's disease, tyrosinemia, Canavan disease, or Creutzfeldt-Jakob disease.

Bush signs rare diseases legislation: new laws address unmet needs of ...

for the distribution of Orfadin(R) for the treatment of Hereditary Tyrosinemia Type I.

Accredo Health, Inc. Announces Record Second Quarter Results; Second ...

org 1,2,3,4,5,7,8,9 TYROSINEMIA, HEREDITARY, HEPATORENAL TYPE/ TYROSINEMIA TYPE I, TYROSYLURIA See also: Kidney Disorders; Liver Disorders Groupe Aide aux Enfants Tyrosinemiques du Quebec Gerard Tremblay, President 3162, Rue Granville Jonquiere, QC CAN G7S 2B9 (418) 548-1580 * gerard.

National resources for specific disabilities

The most frequent of these uncommon conditions is Wilson's disease, a familial disorder of copper metabolism Alpha-1-antitrypsin deficiency and tyrosinemia may appear as chronic hepatitis although other features help in distinguishing these rare conditions from those caused by viruses.

Chronic hepatitis

22, 2002 The FDA notified Swedish Orphan International AB based in Stockholm, Sweden that it has granted marketing approval for Orfadin(R) Capsules (nitisinone) an orphan designated product as an adjunct to dietary restriction of tyrosine and phenylalanine in the treatment of Hereditary Tyrosinemia Type I (HTI).

FDA Approves Drug to Treat Rare Pediatric Liver Disease

Preliminary clinical research studies suggest that quantitation of tyrosine in the first two days of life is extremely unreliable in ascertaining infants with tyrosinemia type 1 (fumarylacetoacetase deficiency).

Potential and pitfalls of NBS, and the reference lab's role