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Tests: L

Test codes, sample requirements and turnaround times for our most requested tests.

Please use the search box below to filter this list

Test name
Lactate (Plasma)
Lactate Dehydrogenase (LDH)
Lactate Pyurvate Ratio
Lactose Intolerance Gene  NEW
Lactose Tolerance Test
Langer-Giedion Syndrome – BOBs (5 days) + karyotype (15 days)
Langer-Giedion Syndrome – BOBs only
Latex Components
LDH lsoenzymes
LDL7 Subfractions
Lead (Blood)
Lead (Urine)
Lead Profile (Hb, ZPP, Lead)
Leber’s Congenital Amaurosis NGS Panel – full sequencing across 32 genes
Lebers Hereditary Optic Neuropathy – m.3460G>A + m.11778G>A + m.14484T>C common mutations
Legionella Antibodies
Legionella Urine Antigen
Leigh Syndrome NGS Panel – full sequencing across 78 genes + deletions/duplications + mitochondrial DNA
Leishmania Antibodies
LEOPARD/Noonan/Cardio-Facio-Cutaneous/Costello Syndromes NGS Panel – full sequencing across 20 genes
Leptospirosis (Weil’s Disease) Abs (IgM)
Leucine Amino Peptidase
Leucocyte Antibody Detection Panel FEMALE
Leucocyte Antibody Detection Panel MALE
Leukaemia Fusion Gene Screening Assay (Q30)
Leukaemia Immunophenotyping
Leukotriene E4
Levetiracetam (Keppra)
Li-Fraumeni Syndrome (p53-related cancer predisposition) – TP53 sequencing + MLPA
Limb-Girdle Muscular Dystrophy (LGMD) NGS Panel – full sequencing across 34 genes
Lipid Profile
Lipid Transfer Proteins
Lipoprotein (a)
Lipoprotein Electrophoresis
Lissencephaly NGS Panel – full sequencing across 14 genes
Listeria Antibody
Liver Fibrosis (Enhanced Liver Fibrosis ELF)
Liver Fibrosis Fibrotest
Liver Function Tests
Liver Immunoblot
Liver Kidney Microsomal Antibodies
Loeys-Dietz Syndrome/Marfan Syndrome/Aortopathy NGS Panel – full sequencing across 26 genes
Long-QT Syndrome / Brugada Syndrome – full sequencing across 34 genes
Lowe (Oculocerebrorenal) Syndrome – OCRL sequencing + large deletions
Lp-PLA2 (PLAC) Test
Lung Disorders NGS Panel –full sequencing across 51 genes
Lupus Anticoagulant and Anticardiolipin Abs
Lupus Anticoagulant only
Luteinising Hormone (LH)
Lyme Disease (Borrelia Abs) IgG, IgM
Lyme Disease (Borrelia Abs) IgM
Lymphocyte Subsets (CD3/CD4/CD8)
Lymphogranuloma Venerium (LGV)
Lynch Syndrome (HNPCC) NGS Panel – full sequencing across 18 genes + deletions/duplications
Lysosomal Disorders NGS Panel – full sequencing across 106 genes
Lysosomal Enzyme Screen