Graphics Library

The Graphics Library contains key pictures and graphics that have been adapted from a review of state newborn screening brochures and requested by parents. All of the graphics are not copyrighted and can be included or adapted to fit within your newborn screening educational materials.

To select graphics for use in your brochure, click on the appropriate category; right-click on the image you would like to use; click on the save button to save the image to your computer; insert the image into your document.

For more information about the Graphics Library, refer to An Introduction to the Message and Graphics Libraries.

Categories:

Pictures:
Baby feet

Inheritance Patterns:
Autosomal recessive inheritance

Metabolic Pathways:
Arginase deficiency metabolic pathway
ASAL (argininosuccinyl-CoA lyase deficiency) metabolic pathway
ASAS (citrullinemia/Argininosuccinate synthetase deficiency) metabolic pathway
BKD (beta-ketothiolase deficiency) metabolic pathway
Carnitine transporter deficiency metabolic pathway
CAT (carnitine/acylcarnitine translocase deficiency) metabolic pathway
CBS (homocystinemia/cystathionine beta-synthase deficiency) metabolic pathway
CPT-1 (carnitine palmitoyl transferase deficiency-type 1) metabolic pathway
CPT-2 (carnitine palmitoyl transferase deficiency-type 2) metabolic pathway
GA-2 (glutaric acidemia-type 2) metabolic pathway
GA-1 (glutaric acidemia type-1) metabolic pathway
HCSD (holocarboxylase synthetase deficiency) metabolic pathway
HMGCoA (3-hydroxy-3-methylglutaryl-CoA lyase deficiency) metabolic pathway
Isobutyryl-CoA dehydrogenase deficiency metabolic pathway
IVA (isovaleric acidemia) metabolic pathway
LCHADD (long chain 3-hydroxyacyl-CoA dehydrogenase deficiency) metabolic pathway
MCADD (medium chain acyl-CoA dehydrogenase deficiency) metabolic pathway
MMA (methylmalonic acidemia) metabolic pathway
MMA+HCU (Methylmalonic Acidemia with Homocystinuria) metabolic pathway
MSUD (maple syrup urine disease) metabolic pathway
PA (propionic acidemia) metabolic pathway
PKU (phenylketonuria) metabolic pathway
SCADD (short chain acyl-CoA dehydrogenase deficiency) metabolic pathway
SCHADD (short chain 3-hydroxyacyl-CoA dehydrogenase deficiency) metabolic pathway
TFP (trifunctional protein deficiency) metabolic pathway
Tyrosinemia metabolic pathway
VLCADD (very long chain acyl-CoA dehydrogenase deficiency) metabolic pathway
3MCC (3-methylcrotonyl-CoA carboxylase deficiency) metabolic pathway
2MBC (2-methylbutyryl-CoA dehydrogenase deficiency) metabolic pathway