Reproductive Genetics tests in Dubai & UAE

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

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Listed price range

2,800.00 AED

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Reproductive Genetics test prices

Showing 1–8 of 8 matching tests.

Reproductive Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3413 AURKC Gene SPGF5 Genetic Test This test detects pathogenic variants in the AURKC gene associated with spermatogenic failure type 5 (SPGF5), a cause of male infertility.	Peripheral whole blood (EDTA), extracted genomic DNA, or dried blood spot on an FTA card	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 AURKC gene"] Parameters [] Preparation [] Indications ["Unexplained azoospermia or severe oligospermia", "Family history of SPGF5", "Carrier screening in consanguineous families"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: N46.0, N46.8 Clinical summary This test detects pathogenic variants in the AURKC gene associated with spermatogenic failure type 5 (SPGF5), a cause of male infertility.
TEST-3388 BMP15 Gene Ovarian Dysgenesis Type 2 (OD2) Genetic Test This test analyzes the BMP15 gene for pathogenic variants associated with Ovarian Dysgenesis Type 2 (OD2) using Next-Generation Sequencing (NGS). It provides definitive molecular c...	Whole Blood / FTA Card / Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BMP15 gene coding regions", "Adjacent intronic boundaries of BMP15 gene"] Parameters [] Preparation ["No specific preparation required"] Indications ["Diagnosis of Ovarian Dysgenesis Type 2", "Familial risk assessment for OD2", "Guidance for fertility preservation", "Guidance for hormone therapy decisions"] Measurement technique Confirm with laboratory Codes LOINC: 21659-3 ICD-10: Q50.0 Clinical summary This test analyzes the BMP15 gene for pathogenic variants associated with Ovarian Dysgenesis Type 2 (OD2) using Next-Generation Sequencing (NGS). It provides definitive molecular confirmation for familial risk assessment and clinical management.
TEST-3409 CATSPER1 Gene (SPGF7) Genetic Test This test detects pathogenic variants in the CATSPER1 gene associated with spermatogenic failure type 7 and male infertility.	Whole Blood (5 mL) or FTA Card	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 CATSPER1 gene", "Spermatogenic failure type 7 genetic cause"] Parameters [] Preparation ["No fasting required", "Do not discontinue prescribed medication or hormone therapy without consulting your physician"] Indications ["Diagnosis of spermatogenic failure type 7", "Evaluation of male infertility", "Guidance for assisted reproductive technologies (ICSI, PGD)"] Measurement technique Confirm with laboratory Codes LOINC: 90228-2 ICD-10: N46.02 Clinical summary This test detects pathogenic variants in the CATSPER1 gene associated with spermatogenic failure type 7 and male infertility.
TEST-3447 KISS1 Gene Hypogonadotropic Hypogonadism Genetic Test This genetic test sequences the entire KISS1 gene to identify variants associated with hypogonadotropic hypogonadism.	Peripheral whole blood (EDTA) or Dried Blood Spot (FTA card)	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["KISS1 gene sequence", "Pathogenic variants in KISS1"] Parameters [] Preparation ["No fasting required", "Discontinue anticoagulants only under medical advice 48 hours before sample collection"] Indications ["Isolated GnRH deficiency", "Normosmic idiopathic hypogonadotropic hypogonadism", "Combined pituitary hormone deficiencies"] Measurement technique Confirm with laboratory Codes LOINC: 78824-5 ICD-10: E23.0, E29.1, Z15.89 Clinical summary This genetic test sequences the entire KISS1 gene to identify variants associated with hypogonadotropic hypogonadism.
TEST-3437 LHCGR Gene Leydig Cell Hypoplasia Type 1 Genetic Test This test detects pathogenic variants in the LHCGR gene associated with Leydig cell hypoplasia type 1, a cause of 46,XY disorders of sex development.	Whole Blood (EDTA) or FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the LHCGR gene", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any bleeding disorders"] Indications ["Newborns with ambiguous genitalia", "Family history of sex development disorders", "Confirmation before sex assignment surgery"] Measurement technique Confirm with laboratory Codes LOINC: 81264-5 ICD-10: E29.1 Clinical summary This test detects pathogenic variants in the LHCGR gene associated with Leydig cell hypoplasia type 1, a cause of 46,XY disorders of sex development.
TEST-3451 NLRP7 Gene Hydatidiform Mole Genetic Test This genetic test detects mutations in the NLRP7 gene associated with a predisposition to recurrent complete hydatidiform moles.	Whole blood (EDTA), 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 ["NLRP7 gene mutations", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["A genetic counselling session to draw a pedigree chart is mandatory before sample collection."] Indications ["Evaluation of individuals with a history of recurrent complete hydatidiform moles", "Family screening for individuals with a known family history of molar pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 93385-8 ICD-10: O01.9, O01.0, O01.1 Clinical summary This genetic test detects mutations in the NLRP7 gene associated with a predisposition to recurrent complete hydatidiform moles.
TEST-3377 SYCP3 Gene Sequencing (SPGF4) Test This test identifies pathogenic variants in the SYCP3 gene associated with spermatogenic failure type 4 (SPGF4), a genetic cause of non-obstructive azoospermia in males.	Peripheral whole blood (EDTA tube)	21–28 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SYCP3 gene variants", "Pathogenic variants causing spermatogenic failure type 4"] Parameters [] Preparation ["No fasting required", "Inform physician about anticoagulant medications"] Indications ["Evaluation of male infertility", "Diagnosis of spermatogenic failure type 4 (SPGF4)"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: N46.0 Clinical summary This test identifies pathogenic variants in the SYCP3 gene associated with spermatogenic failure type 4 (SPGF4), a genetic cause of non-obstructive azoospermia in males.
TEST-3433 ZP1 Gene Oocyte Maturation Defect Genetic Test This genetic test identifies pathogenic mutations within the ZP1 gene associated with oocyte maturation arrest and female infertility.	Peripheral Whole Blood or Extracted DNA	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 ZP1 gene coding region", "Splice site variants"] Parameters [] Preparation ["No special preparation required", "Fasting is not required", "Provide detailed clinical history and family pedigree chart"] Indications ["Women with unexplained infertility", "Recurrent IVF failure", "Primary ovarian insufficiency", "Suspected oocyte maturation arrest based on poor embryo development or empty follicle syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 94086-1 ICD-10: N97.8 Clinical summary This genetic test identifies pathogenic mutations within the ZP1 gene associated with oocyte maturation arrest and female infertility.

Category overview

Reproductive Genetics: overview

Planning for a healthy family starts with a deep understanding of your unique hereditary blueprint, giving expectant parents the ultimate reproductive confidence and peace of mind. As a core pillar of our advanced Molecular Genetics department, comprehensive Reproductive Genetics testing screens prospective parents for carrier status of hundreds of inherited genetic conditions. By utilizing cutting-edge diagnostic technology, this empowering molecular screening provides the critical clarity needed to assess potential risks to future children, safely guiding informed family planning, IVF decisions, and specialized reproductive counseling. Widely respected for compassionate family planning among top diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, uncompromising analytical accuracy, and rapid, dependable reporting. Take an informed, proactive step toward your family’s future—schedule your reproductive genetics testing in UAE, arrange a comfortable clinic or home sample collection, or connect with our dedicated reproductive specialists today.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.