Biochemistry tests in Dubai & UAE

Compare available Biochemistry tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

1,113

Listed price range

450.00–30,000.00 AED

Clinical preparation

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Biochemistry test prices

Showing 811–825 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6088 PPM1K Gene (Maple Syrup Urine Disease, Mild Variant) Genetic Test This test evaluates the PPM1K gene for mutations associated with the mild variant of Maple Syrup Urine Disease (MSUD). It identifies specific genetic alterations linked to impaired...	Peripheral Whole Blood or FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PPM1K gene mutations", "Branched-chain amino acid metabolism pathway"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected mild variant of MSUD", "Family history of MSUD", "Unexplained neurological symptoms", "Need for precise genetic diagnosis for dietary management"] Measurement technique Confirm with laboratory Codes LOINC: 21600-5 ICD-10: E71.0 Clinical summary This test evaluates the PPM1K gene for mutations associated with the mild variant of Maple Syrup Urine Disease (MSUD). It identifies specific genetic alterations linked to impaired branched-chain amino acid metabolism.
TEST-5865 PPOX Gene Porphyria Variegata Genetic Test This test identifies pathogenic variants in the PPOX gene, confirming a diagnosis of variegate porphyria.	Whole Blood (Peripheral)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PPOX gene"] Parameters [] Preparation [] Indications ["Suspected variegate porphyria", "Family screening for variegate porphyria"] Measurement technique Confirm with laboratory Codes LOINC: 58114-3 ICD-10: E80.2 Clinical summary This test identifies pathogenic variants in the PPOX gene, confirming a diagnosis of variegate porphyria.
TEST-2940 Prealbumin (Transthyretin) Test This test measures the level of prealbumin (transthyretin) in the blood to assess acute nutritional status and detect protein-energy malnutrition.	Serum	2–3 weeks (Send-out test; samples processed monthly by the 7th)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Prealbumin (Transthyretin) protein levels", "Acute nutritional status"] Parameters [{"name": "Prealbumin (Transthyretin)", "reference_range": null}] Preparation ["No special fasting is required.", "Inform physician about supplements, medications (especially corticosteroids), or existing medical conditions.", "A duly filled Send Out Consent Form (Form 35) is mandatory."] Indications ["Screening for acute protein-energy malnutrition", "Monitoring nutritional rehabilitation", "Assessing effectiveness of enteral or parenteral feeding", "Insurance medical examinations", "Pre-employment health assessments"] Measurement technique Confirm with laboratory Codes LOINC: 7583-9 ICD-10: E44.0, Z13.89 Clinical summary This test measures the level of prealbumin (transthyretin) in the blood to assess acute nutritional status and detect protein-energy malnutrition.
TEST-2943 Preeclampsia Predictor (sFlt-1:PlGF Ratio) Panel Test This diagnostic test evaluates the ratio of soluble fms-like tyrosine kinase-1 (sFlt-1) to placental growth factor (PlGF) in serum to predict the risk of preeclampsia.	Serum	Same-day (if sample received by 9 AM Tue/Thu/Sat)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["sFlt-1 (soluble fms-like tyrosine kinase-1)", "PlGF (placental growth factor)", "sFlt-1:PlGF ratio"] Parameters [{"name": "sFlt-1", "reference_range": null}, {"name": "PlGF", "reference_range": null}, {"name": "sFlt-1:PlGF Ratio", "reference_range": null}] Preparation ["No special preparation required", "No fasting necessary", "Continue prescribed medications unless instructed otherwise", "Stay well-hydrated"] Indications ["Assessment of short-term preeclampsia risk", "Rule out preeclampsia", "Guide clinical management in pregnancy"] Measurement technique Confirm with laboratory Codes LOINC: 78427-2 ICD-10: O14.9, O14.0, O14.1 Clinical summary This diagnostic test evaluates the ratio of soluble fms-like tyrosine kinase-1 (sFlt-1) to placental growth factor (PlGF) in serum to predict the risk of preeclampsia.
TEST-2950 Pregnenolone Test This diagnostic test evaluates serum pregnenolone levels to assess adrenal gland function and identify potential hormonal imbalances.	Serum	2–3 weeks	2,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Pregnenolone", "Adrenal Gland Function"] Parameters [{"name": "Pregnenolone", "reference_range": null}] Preparation ["Fasting not required", "Avoid exogenous steroids for 24 hours prior to collection", "A mandatory Send Out Consent Form (Form 35) must be completed"] Indications ["Diagnosis of congenital adrenal hyperplasia (CAH)", "Diagnosis of adrenal insufficiency", "Monitoring hormone replacement therapy", "Monitoring anti-aging protocols"] Measurement technique Confirm with laboratory Codes LOINC: 2092-8 ICD-10: E27.9 Clinical summary This diagnostic test evaluates serum pregnenolone levels to assess adrenal gland function and identify potential hormonal imbalances.
TEST-1197 Prenatal Diagnostic Screening by Karyotyping + FISH Test This test provides a definitive analysis of fetal chromosomes to detect aneuploidies and structural abnormalities.	Amniotic fluid or Chorionic Villus Sample (CVS)	15–20 days (preliminary FISH results in 2–3 days)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal number (aneuploidy)", "Chromosomal structure", "Specific chromosomes 13, 18, 21, X, Y"] Parameters [] Preparation ["Full disclosure of medical history, including bleeding disorders or allergies.", "Patients are advised not to discontinue prescribed medication without consulting their doctor."] Indications ["High-risk pregnancies", "Abnormal ultrasound findings", "Positive maternal serum screening"] Measurement technique Confirm with laboratory Codes LOINC: 47230-4 ICD-10: O35.1 Clinical summary This test provides a definitive analysis of fetal chromosomes to detect aneuploidies and structural abnormalities.
TEST-1107 Prenatal Spinal Muscular Atrophy (SMA) Screening Test This test detects deletions, duplications, and point mutations in the SMN1 gene from invasive prenatal specimens using MLPA.	Amniotic Fluid, Chorionic Villi, or Cord Blood	7–10 working days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SMN1 gene deletions", "SMN1 gene duplications", "SMN1 gene point mutations", "SMN1 copy-number variants"] Parameters [] Preparation [] Indications ["Family history of spinal muscular atrophy", "Known carrier status for both parents", "Previous children affected by SMA"] Measurement technique Confirm with laboratory Codes LOINC: 53773-6 ICD-10: Z13.79 Clinical summary This test detects deletions, duplications, and point mutations in the SMN1 gene from invasive prenatal specimens using MLPA.
TEST-4374 PRICKLE2 Gene Progressive Myoclonic Epilepsy Type 5 Genetic Test This genetic test analyzes the PRICKLE2 gene for pathogenic variants associated with progressive myoclonic epilepsy type 5 (EPM5). It uses Next Generation Sequencing (NGS) to detec...	Whole blood (EDTA tube), extracted DNA, or FTA card (peripheral blood specimen)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PRICKLE2 gene", "Single nucleotide variants (SNVs)", "Copy number variations (CNVs)", "Small insertions/deletions (indels)"] Parameters [] Preparation ["Detailed clinical history of progressive myoclonic epilepsy symptoms", "Three-generation pedigree chart", "Genetic counselling is mandatory prior to testing"] Indications ["Suspected diagnosis of progressive myoclonic epilepsy type 5 (EPM5)", "Family history of EPM5", "Need for definitive molecular diagnosis to guide treatment and family planning"] Measurement technique Confirm with laboratory Codes LOINC: 62115-2 ICD-10: G40.309, G40.3 Clinical summary This genetic test analyzes the PRICKLE2 gene for pathogenic variants associated with progressive myoclonic epilepsy type 5 (EPM5). It uses Next Generation Sequencing (NGS) to detect single nucleotide variants, small insertions/deletions, and copy number variations.
TEST-3594 PRKAR1A Gene Sequencing for Primary Pigmented Nodular Adrenocortical Disease Type 1 (Carney Complex) Test This test identifies genetic variants in the PRKAR1A gene associated with Carney complex and primary pigmented nodular adrenocortical disease type 1 (PPNAD1).	Peripheral whole blood (2 × 6 mL EDTA tubes) or FTA card capillary blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRKAR1A gene variants", "Single-nucleotide variants", "Insertions/deletions", "Copy-number variations"] Parameters [] Preparation ["No specific fasting required", "Do not interrupt prescribed therapy without consulting your endocrinologist"] Indications ["Clinical features suggestive of PPNAD or Carney complex", "Family history of endocrine tumours"] Measurement technique Confirm with laboratory Codes LOINC: 90261-5 ICD-10: E24.8, Q85.8 Clinical summary This test identifies genetic variants in the PRKAR1A gene associated with Carney complex and primary pigmented nodular adrenocortical disease type 1 (PPNAD1).
TEST-4197 PRKRA Gene DYT16 Genetic Test This test identifies pathogenic variants in the PRKRA gene associated with DYT16 dystonia-parkinsonism.	Peripheral whole blood, FTA card, or extracted DNA	14–21 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PRKRA gene"] Parameters [] Preparation [] Indications ["Diagnosis of DYT16 dystonia-parkinsonism", "Carrier detection", "Informed reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 52042-9 ICD-10: G24.1 Clinical summary This test identifies pathogenic variants in the PRKRA gene associated with DYT16 dystonia-parkinsonism.
TEST-4161 PRNP Gene Creutzfeldt-Jakob Disease Genetic Test This genetic test analyzes the PRNP gene for mutations linked to Creutzfeldt-Jakob disease, aiding in diagnosis and risk assessment.	Whole Blood, Extracted DNA, or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRNP gene pathogenic variants", "Inherited prion disorder risk"] Parameters [] Preparation ["Genetic Counselling & Pedigree Chart required prior to testing"] Indications ["Family history of CJD", "Unexplained progressive neurological symptoms", "Differential diagnosis of dementia"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: A81.0 Clinical summary This genetic test analyzes the PRNP gene for mutations linked to Creutzfeldt-Jakob disease, aiding in diagnosis and risk assessment.
TEST-4483 PRNP Gene Fatal Familial Insomnia Genetic Test This diagnostic test evaluates the PRNP gene for mutations associated with Fatal Familial Insomnia (FFI), a rare, inherited prion disease.	Whole Blood, Extracted DNA, or Dried Blood Spot on FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRNP gene coding region", "Pathogenic variants (SNVs, indels, copy number changes)"] Parameters [] Preparation ["Pre-test genetic counselling recommended", "Detailed pedigree chart recommended"] Indications ["Family history of Fatal Familial Insomnia", "Clinical suspicion of FFI", "Differential diagnosis of dementia or sleep disorders"] Measurement technique Confirm with laboratory Codes LOINC: 23504-4 ICD-10: A81.83 Clinical summary This diagnostic test evaluates the PRNP gene for mutations associated with Fatal Familial Insomnia (FFI), a rare, inherited prion disease.
TEST-2953 Procainamide and N-Acetylprocainamide (NAPA) Test This test measures the concentration of the antiarrhythmic drug procainamide and its active metabolite NAPA in the blood.	Serum	2–3 Weeks	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Procainamide", "N-Acetylprocainamide (NAPA)"] Parameters [{"name": "Procainamide", "reference_range": null}, {"name": "N-Acetylprocainamide (NAPA)", "reference_range": null}] Preparation ["Collect sample just before next dose", "Sample must be refrigerated, never frozen"] Indications ["Therapeutic drug monitoring for procainamide", "Management of ventricular tachycardia", "Assessment of drug efficacy and toxicity"] Measurement technique Confirm with laboratory Codes LOINC: 3528-7 ICD-10: Z51.81 Clinical summary This test measures the concentration of the antiarrhythmic drug procainamide and its active metabolite NAPA in the blood.
TEST-2967 Proinsulin Test This diagnostic test evaluates the level of proinsulin in the blood, a precursor to insulin, to aid in the detection of specific pancreatic tumors and metabolic conditions.	Serum (fasting)	2–3 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Proinsulin levels", "Beta-cell function"] Parameters [{"name": "Proinsulin", "reference_range": null}] Preparation ["Overnight fast (10–12 hours)", "Drink only plain water", "Avoid strenuous exercise for 24 hours", "Sign Send Out Consent Form (Form 35)"] Indications ["Detection of insulinoma", "Evaluation of pancreatic neuroendocrine tumors", "Assessment of high-risk metabolic syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 2599-6 ICD-10: C25.4, C25.9, Z15.09 Clinical summary This diagnostic test evaluates the level of proinsulin in the blood, a precursor to insulin, to aid in the detection of specific pancreatic tumors and metabolic conditions.
TEST-3758 PROKR2 Gene Hypogonadotropic Hypogonadism Type 3 (with or without Anosmia) Genetic Test This test evaluates the PROKR2 gene for pathogenic variants associated with hypogonadotropic hypogonadism type 3.	Whole Blood or Dried Blood Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PROKR2 gene", "Single nucleotide variants", "Small deletions/duplications"] Parameters [] Preparation [] Indications ["Idiopathic hypogonadotropic hypogonadism", "Suspected Kallmann syndrome", "Family planning in affected families"] Measurement technique Confirm with laboratory Codes LOINC: 94716-0 ICD-10: E23.0 Clinical summary This test evaluates the PROKR2 gene for pathogenic variants associated with hypogonadotropic hypogonadism type 3.

Category overview

Biochemistry: overview

Seeking clarity about your body's essential functions is vital for long-term well-being. At DNA Labs UAE, our Biochemistry services utilize advanced automated analyzers to evaluate enzymes, proteins, and metabolites in your blood. Whether you need routine metabolic panels or specialized biochemical testing in the UAE, these tests provide critical data to guide your physician's medical plan. As a leading diagnostic lab in Dubai and the UAE, we guarantee strict confidentiality and rapid, accurate turnaround times. Take charge of your health today. Explore our biochemistry diagnostics below, schedule a convenient home sample collection, or contact our specialists to book your test.

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Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

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