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Hypermethioninemia
Results: 12

#	Item
1	AMINO ACID DISORDERS Karla J Matteson, PhD, FACMG University of Tennessee Genetic Center, Knoxville Outcome without screening: The amino acid disorders are a collection of disorders that involve enzyme deficiencies that Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2006-10-30 12:08:43 Rare diseases Phenylketonuria Newborn screening Urea cycle disorder Hypermethioninemia Maple syrup urine disease Amino acid Protein Citrullinemia Health Medicine Genetic genealogy
2	Homocystinuria Homocystinuria is an autosomal recessive disorder of methionine metabolism. The most common cause of homocystinuria is a deficiency of the amino acid cystathionine B-synthase. Due to this deficiency, eleva Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:06 Homocystinuria Homocysteine Marfan syndrome Methionine Cystathionine beta synthase Cystinuria Newborn screening Hypermethioninemia Health Chemistry Genetic genealogy
3	NEWBORN SCREENING FACT SHEET Hypermethioninemia (MET) What is it? Hypermethiuoninemia (also known as MET) is an inherited amino acid disorder. People with Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:53 Pediatrics Medical specialties Epidemiology Newborn screening Medical genetics Hypermethioninemia Bismarck North Dakota Medicine Health Rare diseases
4	Overview of Newborn Screening for Amino Acid Disorders – For Parents What is newborn screening? Before babies go home from the nursery, they have a small amount of blood taken from their heel to test for a group of con Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-22 10:08:32 Amino acid Maple syrup urine disease Phenylketonuria Newborn screening Urea cycle disorder Protein Metabolism Hypermethioninemia Isobutyryl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
5	Hypermethioninemia (MET) What problems can Hypermethioninemia cause? What is a positive newborn screen? Newborn screening is done on tiny samples of Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 20:45:56 Rare diseases Medical tests Epidemiology Newborn screening Screening Protein Hypermethioninemia Infant 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Pediatrics
6	AMINO ACID DISORDERS Karla J Matteson, PhD, FACMG University of Tennessee Genetic Center, Knoxville Outcome without screening: The amino acid disorders are a collection of disorders that involve enzyme deficiencies that Add to Reading List Source URL: health.tn.gov Language: English - Date: 2006-10-30 12:08:43 Rare diseases Phenylketonuria Newborn screening Urea cycle disorder Hypermethioninemia Maple syrup urine disease Amino acid Protein Citrullinemia Health Medicine Genetic genealogy
7	Microsoft Word - mso20.doc Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2007-09-14 08:02:14 Rare diseases Hypermethioninemia Newborn screening Medical genetics 2-Methylbutyryl-CoA dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medicine Health Genetic genealogy
8	American College of Medical Genetics ACT SHEET Newborn Screening ACT Sheet Add to Reading List Source URL: www.babysfirsttest.org Language: English - Date: 2013-01-09 15:50:02 Newborn screening Pediatrics Medical terms Homocystinuria Homocysteine Maternal and Child Health Bureau Medical guideline Cystathionine beta synthase Hypermethioninemia Health Medicine Epidemiology
9	Microsoft Word - mso20.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 08:02:14 Rare diseases Hypermethioninemia Newborn screening Medical genetics 2-Methylbutyryl-CoA dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medicine Health Genetic genealogy
10	AMINO ACID DISORDERS Karla J Matteson, PhD, FACMG University of Tennessee Genetic Center, Knoxville Outcome without screening: The amino acid disorders are a collection of disorders that involve enzyme deficiencies that Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2006-10-30 12:08:43 Rare diseases Phenylketonuria Newborn screening Urea cycle disorder Hypermethioninemia Maple syrup urine disease Amino acid Protein Citrullinemia Health Medicine Genetic genealogy