Searched for "newborn screening".
70
results
found
on Genetics Home Reference.
Showing results 1 to 20.
- newborn screening definition
- What are the types of genetic tests? in the Handbook
Found in subheading: Newborn screening
- phenylketonuria condition summary
Found: ...detected shortly after birth by newborn screening, and treatment is started promptly....
- 2-methylbutyryl-CoA dehydrogenase deficiency condition summary
Found: ...deficiency through newborn screening are usually asymptomatic....
- medium-chain acyl-CoA dehydrogenase deficiency condition summary
Related term: newborn screening
- short-chain acyl-CoA dehydrogenase deficiency condition summary
Related term: newborn screening
- very long-chain acyl-CoA dehydrogenase deficiency condition summary
Related term: newborn screening
- 17β-hydroxysteroid dehydrogenase type 10 deficiency condition summary
Related term: newborn screening
- 21-hydroxylase deficiency condition summary
Related term: newborn screening
- 3-hydroxyacyl-CoA dehydrogenase deficiency condition summary
Related term: newborn screening
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency condition summary
Related term: Newborn screening
- 3-methylcrotonyl-CoA carboxylase deficiency condition summary
Related term: newborn screening
- 3-methylglutaconic aciduria condition summary
Related term: newborn screening
- adenosine deaminase deficiency condition summary
Related term: newborn screening
- alpha thalassemia condition summary
Related term: newborn screening
- arginase deficiency condition summary
Related term: newborn screening
- argininosuccinic aciduria condition summary
Related term: newborn screening
- beta-ketothiolase deficiency condition summary
Related term: newborn screening
- beta thalassemia condition summary
Related term: newborn screening
- biotinidase deficiency condition summary
Related term: newborn screening