Pediatric Laboratory Testing Services
ARUP offers a test menu that accommodates
over 99 percent of pediatric testing requests for the diagnosis and
management of conditions that affect the healthy growth and
development of the pediatric patient. With a large percentage
of testing performed at ARUP, children’s hospitals can be more
operationally efficient with their referral testing.
| Cystic Fibrosis | |
|---|---|
| 0050756 | Cystic Fibrosis, Atypical |
| 0051110 | Cystic Fibrosis, Full Gene Analysis |
| 0056040 | Cystic Fibrosis, Mutation Panel |
| 0051150 | Cystic Fibrosis Mutation Panel with Reflex to CFTR Full Gene Analysis |
| Developmental Delay Evaluation | |
| 0051113 | Angelman Syndrome |
| 0097615 | Chromosome Analysis, FISH-Metaphase |
| 0097640 | Chromosome Analysis, Peripheral Blood |
| 0097615 | Chromosome Analysis, FISH-Metaphase |
| 0040011 | Fragile X Syndrome, DNA Testing |
| 0093019 | Mitochondrial DNA (mtDNA), Whole Genome Scanning and Identification (Mito-ScanGx™) |
| 0051116 | Prader-Willi Syndrome |
| 0051618 | Rett Syndrome (MECP2), Deletion & Duplication |
| 0051614 | Rett Syndrome (MECP2), Full Gene Analysis |
| 0051378 | Rett Syndrome (MECP2), Full Gene Sequencing |
| Drugs, Toxins, and Trace Elements | |
| 0090050 | Caffeine |
| 0020596 | Copper, Serum Free (Direct) |
| 0090110 | Ethylene Glycol |
| 0090003 | Flecainide 1 |
| 0090177 | Lamotrigine 2 |
| 0020745 | Lead, Blood (Capillary) |
| 0092516 | Neonatal 9 drug panel, meconium with reflex to confirmation: Amphetamines, Barbiturates, Benzodiazepines, Cannabinoids, Cocaine, Methadone, Opiates, Phencyclidine, and Propoxyphene |
| 0098467 | Sirolimus 3 |
| 0090265 | Theophylline |
| 0020462 | Zinc, Urine |
| Endocrine Disorders | |
| 0070005 | 17-Hydroxyprogesterone |
| 0092330 | Adrenal Steroid Quantitative Panel by LC-MS/MS, Serum |
| 0097222 | Cortisol Urine Free by LC-MS/MS |
| 0092100 | Cortisol/Cortisone Urine Free by LC-MS/MS |
| 0070040 | Dehydroepiandrosterone Sulfate, Serum |
| 0093247 | Estradiol, Serum by LC-MS/MS |
| 0093248 | Estrogens, Serum Fractionated by LC-MS/MS |
| 0093249 | Estrone, Serum by LC-MS/MS |
| 0070055 | Follicle Stimulating Hormone, Serum |
| 0070080 | Growth Hormone |
| 0070060 | Insulin-Like Growth Factor Binding Protein-3 |
| 0070125 | Insulin-Like Growth Factor I |
| 0070093 | Luteinizing Hormone, Serum |
| 0092334 | Pregnenolone by MS/MS, Serum |
| 0081059 | Testosterone Free, Females or Children by LC-MS/MS |
| 0081058 | Testosterone, Females or Children by LC-MS/MS |
| 0081056 | Testosterone, Free & Total (Includes SHBG), Females or Children by LC-MS/MS |
| 0093244 | Thyroxine, Free (Free T4) by LC-MS/MS |
| 0093243 | Triiodothyronine, Free (Free T3) by LC-MS/MS |
| 0080379 | Vitamin D, 25-Hydroxy |
| Immunologic and Autoimmune Disorders | |
| Search Tests | Allergen Testing by ImmunoCAP® |
| Search Tests | Complement Component Testing |
| 0050779 | Diphtheria, Tetanus, and H. Influenzae b Antibodies, IgG |
| 0051357 | Gliadin Peptide Antibody, IgA |
| 0050345 | Immunoglobulin E |
| 0050577 | Immunoglobulin G Subclasses (1, 2, 3, 4) |
| 0095899 | Lymphocyte - Congenital Immunodeficiencies |
| 0096056 | Lymphocyte Antigen & Mitogen Proliferation Panel |
| 0051584 | Lymphocyte Antigen & Mitogen Proliferation Panel with Cytokine Response to Mitogens |
| 0096657 | Neutrophil Oxidative Burst Assay (DHR) |
| 0095921 | Neutrophil Receptor Profile |
| 0050725 | Streptococcus pneumoniae Antibodies, IgG (14 serotypes) |
| 0097709 | Tissue Transglutaminase Antibody, IgA |
| Inherited Genetic Disorders | |
| 0051266 | Achondroplasia Mutation |
| 0051256 | alpha-1-Antitrypsin Genotype & Phenotype |
| 0051415 | Ashkenazi Jewish Panel 4 |
| 0051288 | Beta-2-Adrenergic Receptor Gene Haplotyping |
| 0051383 | Connexin 26 (GJB2), 35delG Mutation Detection |
| 0051374 | Connexin 26 (GJB2), Sequencing |
| 0051176 | Galactosemia, GALT Gene Mutations |
| 0051476 | Glaucoma (Primary Congenital), CYP1B1 Sequencing |
| Search Tests | Hereditary Hemorrhagic Telangiectasia (HHT) Molecular Testing |
| 0051367 | Hypochondroplasia |
| 0051390 | Multiple Endocrine Neoplasia Type 2 (MEN2), RET Gene Mutations |
| Search Tests | Thanatophoric Dysplasia Type I & II, FGFR3 Gene Mutations3 |
| Inherited Hematological Disorders | |
| 0051495 | Alpha Thalassemia, HBA1 & HBA2 Gene Deletions |
| 0050578 | Beta Globin (HBB) Full Gene Sequencing |
| 0030095 | Factor VIII, Activity |
| 0030100 | Factor IX, Activity |
| 0050613 | Hemoglobin (Hb) A2 & F by Column |
| 0050528 | Hemoglobin Bart |
| 0050610 | Hemoglobin Evaluation with Reflex to Electrophoresis and/or RBC Solubility |
| 0030002 | von Willebrand Multimeric Panel |
| Inherited Metabolic Disorders | |
| 0040033 | Acylcarnitine Quantitative Profile, Plasma |
| 0081170 | Acylglycines, Quantitative, Urine |
| 0080710 | Amino Acids Quantitative, Plasma |
| 0093362 | Biotinidase, Serum (with paired normal control) |
| 0080068 | Carnitine, Free & Total (Includes Carnitine, Esterified) |
| 0081110 | Carnitine Panel |
| 0080512 | Carnitine Transport, Fibroblasts |
| 0080351 | Ehlers-Danlos Syndrome Type VI Screen |
| 0081296 | Galactose-1-Phosphate, in Red Blood Cells |
| 0051346 | Galactosemia Full Gene Analysis |
| 0051175 | Galactosemia, Galactose-1-Phosphate Uridyltransferase & GALT Gene Mutations |
| 0099869 | Homocysteine, Total |
| 0051205 | Medium Chain Acyl-CoA dehydrog(enase) (A985G, T199C) |
| 0098389 | Organic Acids, Urine |
| 0092458 | Orotic Acid, Urine |
| Leukemia, Lymphoma, and Oncology | |
| 0097605 | Chromosome Analysis, Bone Marrow |
| 0097635 | Chromosome Analysis, Leukemic Blood |
| 0051220 | Ewing Sarcoma by RT-PCR |
| 0080422 | Homovanillic Acid (HVA), Urine |
| 0095244 | Leukemia/Lymphoma Phenotyping (Bone Marrow) |
| 0096299 | Leukemia/Lymphoma Phenotyping (Whole Blood) |
| 0080436 | Metanephrines, Urine |
| 0050446 | MLL-AF4, t(4;11) Translocation by RT-PCR |
| 0049235 | N-myc by FISH |
| 0040113 | PAX-FKHR Translocation by RT-PCR |
| 0056008 | TEL-AML1, t(12;21) Translocation by RT-PCR |
| 0080421 | Vanillylmandelic Acid (VMA), Urine |
| Molecular Infectious Disease Testing | |
| 0065080 | Bordetella pertussis/parapertussis by PCR |
| Search Tests | Cytomegalovirus DNA by PCR (Qualitative or Quantitative) |
| 0050249 | Enterovirus Detection by RT-PCR |
| 0050246 | Epstein-Barr Virus by PCR |
| 0060256 | Mycoplasma pneumoniae by PCR |
| 0060043 | Parvovirus B 19, by PCR |
| Serological Infectious Disease Testing | |
| 0050808 | Bordetella pertussis Antibodies, IgA, IgG, & IgM |
| 0050622 | Cytomegalovirus Antibodies, IgG & IgM |
| Search Tests | Epstein-Barr Virus Antibody Testing |
| Search Tests | Hepatitis Virus Testing |
| Search Tests | Herpes Simplex Virus Type 1 and/or 2 Antibody Testing |
| 0050375 | Measles (Rubeola) Antibodies, IgG & IgM |
| Search Tests | Mumps Virus Antibody Testing |
| 0065120 | Parvovirus B 19 Antibodies, IgG & IgM |
| 0050552 | Rubella Antibodies, IgG & IgM |
| Search Tests | TORCH Antibody Testing |
| 0050521 | Toxoplasma gondii Antibodies, IgG & IgM |
| 0050162 | Varicella-Zoster Virus Antibodies, IgG & IgM |
| Other Testing | |
| 0095229 | Cystatin C, Serum |
| Search Tests | Maternal Serum Screening |
| 0080525 | Vitamin A (Retinol), Serum or Plasma |
| 0080521 | Vitamin E, Serum or Plasma |
| 0020612 | Xylose Absorption Test (Child) |
| 1 See the ARUP Laboratory Test Directory for other antiarrhythmic drugs. | |
| 2 See the ARUP Laboratory Test Directory for other anticonvulsant drugs. | |
| 3 See the ARUP Laboratory Test Directory for other immunosuppressant drug.s | |
| 4 See the ARUP Laboratory Test Directory to order individual components of the Ashkenazi Jewish Panel. |
Pediatric Medical Consultation
Consultations for anatomic and clinical pathology
are provided by ARUP’s medical directors and
clinical consultants. These staff members hold
faculty appointments in the Department of
Pathology at the University of Utah School of
Medicine, and many are board-certified pathologists.
They conduct research and remain current on
diagnostic and therapeutic issues through their
involvement in academics and clinical practice.
Test Interpretation
ARUP Consult®, the physician’s guide to
laboratory test selection and interpretation, provides background
information, test- ordering suggestions, and concise diagnostic advice
on disease-related topics. It is co-authored by ARUP’s experts and
includes recommendations congruent with national guidelines and
diagnostic algorithms.
Pediatric Projects
CHILDx—Children’s Health Improvement through Laboratory
Diagnostics
ARUP Institute for Clinical and Experimental Pathology®
Pediatric Reference Interval Study