Tyrosinemia
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Tyrosinemia - Genetics Home Reference
Tyrosinemia is a genetic disorder characterized by elevated blood levels of the amino acid tyrosine, a building block of most proteins. ...
ghr.nlm.nih.gov/condition=tyrosinemia
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Tyrosinemia Hereditary Symptoms & Info
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Tyrosinemia: eMedicine Pediatrics: Genetics and Metabolic Disease
Sep 1, 2009 ... Overview: Elevated blood tyrosine levels are associated with several clinical entities. The term tyrosinemia was first given to a clinical ...
emedicine.medscape.com/article/949816-overview
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Tyrosinemia - Wikipedia, the free encyclopedia
Apr 6, 2009 ... Tyrosinemia (or "Tyrosinaemia") is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid ...
en.wikipedia.org/wiki/Tyrosinemia
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Tyrosinemia Type I
Article describes tyrosinemia type I, its symptoms, diagnosis, and treatment.
rarediseases.about.com/od/rarediseasest/a/tyrosine...
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Tyrosinemia - NEWBORN SCREENING
Oct 8, 2007 ... This fact sheet contains general information about tyrosinemia 1. Every child is different and some of these facts may not apply to your ...
www.newbornscreening.info/Parents/aminoaciddisorde...
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Tyrosinemia
Tyrosinemia Type I was described in 1957 and is caused by deficiency of fumarylacetoacetate hydrolase (FAH). While a predominance of patients are of French ...
www.perkinelmergenetics.com/Tyrosinemia.htm
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Newborn Screening Program - Tyrosinemia
Note: Some cases of tyrosinemia may not be detected by newborn screening when specimens are collected in the first few days of life, as tyrosine levels may ...
www.idph.state.il.us/HealthWellness/fs/tyrosinemia...
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OMIM - TYROSINEMIA, TYPE I
MIM +276700 ? Text ? Animal Model ? Allelic Variants ? View List ? See Also ? References ? Contributors ? Creation Date ? Edit History ? Clinical Synopsis ...
www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276700
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Tyrosinemia type II - Wikipedia, the free encyclopedia
Tyrosinemia type II (also known as "Oculocutaneous tyrosinemia," and "Richner-Hanhart syndrome" [1]:543) is an autosomal recessive condition with onset between ages 2 and 4 years ...
en.wikipedia.org/wiki/Tyrosinemia_II
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Disease Information from NORD, National Organization for Rare ...
National Organization for Rare Disorders is dedicated to helping people with ... Tyrosinemia type I is a rare genetic metabolic disorder characterized by lack of ...
www.rarediseases.org/search/rdbdetail_abstract.htm...
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Tyrosinemia definition - Medical Dictionary definitions of ...
Online Medical Dictionary and glossary with medical definitions ... Tyrosinemia type I is inherited as an autosomal recessive disorder and causes ...
www.medterms.com/script/main/art.asp?articlekey=21...
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Tyrosinemia Type 1 -- GeneReviews -- NCBI Bookshelf
GeneReviews designates a molecular genetic test as clinically available only if the test is listed in the GeneTests Laboratory Directory by either a US CLIA-licensed laboratory or ...
www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&p...
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Open Directory - Health: Conditions and Diseases: Rare Disorders ...
Mar 1, 2009 ... the entire directory, only in Rare_Disorders/Tyrosinemia ... NORD: Tyrosinemia, Hereditary - Offers the synonyms, a general discussion and ...
www.dmoz.org/Health/Conditions_and_Diseases/Rare_D...
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Newborn With Kidney Problems
Newborn With Kidney Problems; Get Answers From Doctors & Patients.
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