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Lab test catalogue
Browse or search our laboratory test catalogue for more information on the tests and diagnostic services offered by the Department of Paediatric Laboratory Medicine (DPLM) at SickKids.
Our goal is to make the process of finding and ordering a test as simple as possible. Tests are categorized by lab discipline. Within each test specific page are the specimen requirements, ordering information, interpretation details and appropriate requisitions.
Using the search box at the top of the page, you are able to search by entering:
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Clinical Biochemistry - General
- 25-Hydroxyvitamin D
- Alpha-Fetoprotein (AFP)
- Anti-TPO Antibody, plasma or serum
- Beta-Hydroxybutyrate, CSF
- Beta-Hydroxybutyrate, serum (or plasma)
- Cortisol, serum or plasma
- Fatty Acids, Free, serum
- Fecal Elastase, stool
- Ferritin, serum or plasma
- Folate, erythrocytes
- Follicle Stimulating Hormone (FSH), serum or plasma
- Free T4, serum
- Insulin-like Growth Factor 1 (IGF-1)
- Lithium, serum
- Luteinizing Hormone (LH), serum and plasma
- Osmolality, plasma or serum
- Osmolality, urine
- Parathyroid Hormone (PTH)
- Prolactin, serum and plasma
- Thyroid-Stimulating Hormone (TSH), serum or plasma
- Triiodothyronine, Total, serum and plasma
- Vitamin D, 1, 25 Dihydroxy, plasma or serum
Clinical Biochemistry - Immunology
Clinical Biochemistry - Metabolic Diseases
- Amino Acids, Blood
- Amino Acids, CSF
- Amino Acids, Urine
- Breath Hydrogen
- Carnitine
- Carnitine, urine
- Creatine Disorders Panel, urine
- Galactosemia Screen
- Glycolipids TLC, urine
- Hyperoxaluria Panel (Currently not available)
- Maple Syrup Urine Syndrome (DBS)
- Mitochondrial Diseases
- Mucopolysaccharides Screen, urine
- Oligosaccharides, urine
- Organic Acids, Urine
- Orotic Acid, Urine
- Oxalate
- Phenylalanine/Tyrosine (DBS)
- Sialic Acid, Urine
- Succinylacetone, Urine
- Sulfatides, Urine
- Sulfocysteine, urine
- Tay-Sachs Disease Carrier Test (Enzyme Analysis)
Clinical Biochemistry - TDM & Toxicology
- Acetaminophen, plasma or serum
- Amikacin, plasma or serum
- Broad Spectrum Drug Screen, plasma or serum
- Broad Spectrum Drug Screen, urine
- Cannabinoid Metabolite, urine
- Carbamazepine, plasma or serum
- Carbamazepine-10,11-Epoxide
- Digoxin, plasma or serum
- Ethosuximide
- Gentamicin, plasma or serum
- Lamotrigine
- Methotrexate, plasma or serum
- Phenobarbital, plasma or serum
- Phenytoin, plasma or serum
- Primidone
- Sedatives-Barbiturates-Hypnotics Screen, plasma or serum
- Tobramycin, plasma or serum
- Valproate, plasma or serum
- Vancomycin, plasma or serum
- Voriconazole, plasma
Genome Diagnostics - Cytogenetics
- Ataxia Telangiectasia /Nijmegen Breakage Syndrome
- Bloom Syndrome
- Fanconi Anemia (DEB, MMC)
- Fluorescence in situ Hybridization (FISH) - Blood
- Fluorescence in situ Hybridization (FISH) - Bone Marrow Aspirate/Unstimulated Peripheral Blood
- Fluorescence in situ Hybridization (FISH) - Tissue
- Fluorescence in situ Hybridization (FISH) - Tumour (Fresh/FFPE)
- Genomic SNP Microarray - Blood
- Karyotype, GTG-banding - Bone Marrow Aspirate
- Karyotype, GTG-banding -Tissue
- Karyotype, GTG-banding -Tumour
- SNP microarray – OncoScan – FFPE tumour tissue
Genome Diagnostics - Molecular Genetics
- 22q11.2 Deletion Syndrome
- Achondroplasia / Hypochondroplasia
- Angelman Syndrome
- Ashkenazi Jewish Screening Panel
- Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis Panel: Sequencing
- Autoinflammatory Disease Panel: Recurrent Fever Syndrome
- Autoinflammatory Disease: Hemophagocytic Lymphohistiocytosis (HLH) panel
- Becker Muscular Dystrophy
- Beckwith-Wiedemann Syndrome
- Bloom Syndrome: BLM Recurrent Mutations
- Bone Marrow Transplant Testing (BMT)
- Branchio-Oto-Renal Syndrome: EYA1
- Caffey Disease: COL1A1 Recurrent Mutation
- Canavan Disease
- CHARGE Syndrome: CHD7
- Cherubism: SH3BP2
- Congenital Muscular Dystrophies Panel: Sequencing
- Connective Tissue Disease: Bone Involvement Panel
- Craniosynostosis Molecular Analysis
- Cystic Fibrosis
- DNA Banking
- Dopamine Beta-Hydroxylase Deficiency: DBH Sequencing
- Duchenne Muscular Dystrophy
- Fabry Disease
- Familial Dysautonomia
- Fanconi Anemia Group C: FANCC Recurrent Mutations
- Focal Segmental Glomerulosclerosis Panel
- Fragile X Syndrome
- FRAXE
- Hearing Loss, Non-Syndromic (GJB2 and GJB6)
- Hearing Loss: Pendred Syndrome (SLC26A4)
- Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel
- Hereditary Hearing Loss: Stickler Syndrome
- Hereditary Hearing Loss: Syndromic Hearing Loss - Treacher Collins syndrome, Waardenburg syndrome, Norrie syndrome, Alport syndrome
- Hereditary Hearing Loss: Usher Syndrome
- Hereditary Hemorrhagic Telangiectasia: ACVRL1, ENG
- Hereditary Hemorrhagic Telangiectasia: SMAD4 Sequencing
- Hereditary Spastic Paraplegia: Autosomal Dominant
- Hereditary Spastic Paraplegia: Autosomal Recessive
- Hereditary Spastic Paraplegia: X-Linked
- Hunter Disease
- Identity Testing - MCC Studies, Zygosity
- Mucolipidosis Type 4: MCOLN1 Recurrent Mutations
- Neurofibromatosis Type 1/Legius Syndrome
- Neuronal Ceroid Lipofuscinoses
- Niemann Pick Disease Type A and B: SMPD1 Recurrent Mutations
- Noonan Syndrome and RASopathies
- Prader-Willi Syndrome
- Russell Silver Syndrome
- Shwachman-Diamond Syndrome
- Simpson-Golabi-Behmel Syndrome: GPC3 Sequencing, GPC3 and GPC4 Deletion/Duplication Analysis
- Spinal and Bulbar Muscular Atrophy (SBMA)
- Spinal Muscular Atrophy
- Thanatophoric Dysplasia (Type I & II)
- Trismus-Pseudocamptodactyly Syndrome: MYH8 Sequencing
- X-Inactivation Analysis
Haematopathology
- Autoimmune Lymphoproliferative Syndrome (ALPS)
- CD34 Enumeration, Apheresis
- CD34 Enumeration, Bone Marrow
- CD45 RA/RO
- Hereditary Spherocytosis Screening
- Minimal Residual Disease (MRD) Day 29
- Minimal Residual Disease (MRD) Day 8
- NK Degranulation Assay
- Perforin Protein Expression
- Platelet-Membrane Glycoprotein Expression
- Recent Thymic Emigrants
- T Cell Subsets, CD3/CD4/CD8
Microbiology - Molecular
- Adenovirus PCR - Autopsy/Biopsy
- Adenovirus PCR - BAL (Broncho-Alveolar Lavage)
- Adenovirus PCR - Corneal Scrape
- Adenovirus PCR - Eye
- Adenovirus PCR - Urine
- Bacterial meningitis PCR
- Bartonella Group PCR - CSF
- CMV, EBV, HHV 6 by PCR - Autopsy/Biopsy
- CMV, EBV, HHV 6 by PCR - Blood
- CMV, EBV, HHV 6 by PCR - Body Fluid
- CMV, EBV, HHV 6 by PCR - CSF
- Enterovirus by RT PCR - Blood
- Enterovirus by RT PCR - CSF
- HHV 6A & HHV 6B by PCR
- HHV 7 by PCR
- HSV 1 & 2, VZV by PCR - Blood
- HSV 1 & 2, VZV by PCR - Body Fluid
- HSV 1 & 2, VZV by PCR - CSF
- Human Herpes Group (HSV 1 & 2, VZV) by PCR - Lesion Scraping
- Human Herpes Group (HSV 1& 2, VZV) by PCR - Oral
- Kingella kingae PCR - Joint/Synovial Fluid
- Parechovirus by RT-PCR - Blood
- Parvovirus B19 by PCR
- West Nile Virus PCR - CSF
Customer Service
Toll Free: 1-855-381-3212
Local: 416-813-7200
Browse tests by laboratory
Customer Service
Toll Free: 1-855-381-3212
Local: 416-813-7200