<--- Back to Details
First PageDocument Content
Genetic genealogy / Newborn screening / Propionic acidemia / Methylmalonic acidemia / Isovaleric acidemia / Biotinidase deficiency / Maple syrup urine disease / Glutaric aciduria type 1 / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine
Date: 2011-07-21 16:18:35
Genetic genealogy
Newborn screening
Propionic acidemia
Methylmalonic acidemia
Isovaleric acidemia
Biotinidase deficiency
Maple syrup urine disease
Glutaric aciduria type 1
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Health
Rare diseases
Medicine

Agency of Human Services  Division of Maternal and Child Health  Children with Special Health Needs  Vermont Newborn Screening Program REFUSAL TO CONSENT TO NEWBORN SCREENING

Add to Reading List

Source URL: healthvermont.gov

Download Document from Source Website

File Size: 76,80 KB

Share Document on Facebook

Similar Documents

Medical genetics / Newborn screening / Isovaleric acidemia / Propionic acidemia / Methylmalonic acidemia / Fatty-acid metabolism disorder / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Galactosemia / Malonyl-CoA decarboxylase deficiency / Health / Rare diseases / Genetic genealogy

Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings

DocID: 12jOC - View Document

Rare diseases / Fatty-acid metabolism disorder / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Glutaric aciduria type 1 / Carnitine / Biotinidase deficiency / Biotin / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Genetic genealogy / Medical genetics

Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition Incidence

DocID: Z5KR - View Document

Rare diseases / Pediatrics / Inborn errors of carbohydrate metabolism / Hepatology / Epidemiology / Newborn screening / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Systemic primary carnitine deficiency / Mitochondrial trifunctional protein deficiency / Health / Medicine / Genetic genealogy

Microsoft Word - pocket facts.docx

DocID: NT9O - View Document

Medical genetics / Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Propionic acidemia / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Acyl CoA dehydrogenase / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy

Disorders and Reference Ranges

DocID: KTuv - View Document

Medical genetics / Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Propionic acidemia / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Acyl CoA dehydrogenase / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy

Disorders and Reference Ranges

DocID: KToy - View Document