Ciliopathies Panel NGS Genetic Test sale cost 4400 AED
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Ciliopathies Panel NGS Genetic Test Cost

Original price was: 6,000 د.إ.Current price is: 4,400 د.إ.

-27%

The “Ciliopathies Panel NGS Genetic Test” offered by DNA Labs UAE is a comprehensive diagnostic tool designed to detect genetic mutations associated with ciliopathies, a group of rare, genetically heterogeneous disorders. These disorders are caused by dysfunction in cilia, the microscopic, hair-like structures on the surface of cells that play crucial roles in cell movement, signaling, and coordination. Ciliopathies can affect multiple organ systems, leading to a wide range of symptoms and conditions, including kidney disease, retinal degeneration, brain malformations, and more.

This panel utilizes Next-Generation Sequencing (NGS) technology, a cutting-edge approach that allows for the simultaneous sequencing of multiple genes. This is particularly useful for diseases like ciliopathies, where mutations in any of several different genes can result in similar clinical manifestations. The NGS method enhances the accuracy, efficiency, and comprehensiveness of genetic testing, enabling healthcare providers to make more informed decisions regarding diagnosis, treatment, and management of these complex conditions.

The cost of the Ciliopathies Panel NGS Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the detailed analysis of a broad spectrum of genes associated with ciliopathies, offering patients and their families critical insights into their genetic health. By identifying specific genetic mutations, the test can help in confirming a diagnosis, understanding the risk of developing certain conditions, and in some cases, guiding targeted therapy and management strategies.

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Ciliopathies Panel NGS Genetic Test

Are you or your loved ones experiencing symptoms related to ciliopathies? The Ciliopathies Panel NGS Genetic DNA Test offered by DNA Labs UAE can help diagnose and provide valuable insights into these genetic disorders. Read on to learn more about the test and its cost.

Test Name: Ciliopathies Panel NGS Genetic DNA Test

Components Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information

Before undergoing the Ciliopathies Panel NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with various ciliopathy disorders. Some of the genes associated with ciliopathies include ACVR2B, AGPS, AHI1, ALPL, ANKH, ANO5, ARHGAP31, ARL13B, ARL6, ARMC4, ARSL, ATR, and many more.

Test Details

The Ciliopathies Panel NGS Genetic DNA Test is a comprehensive genetic test that analyzes an individual’s DNA for mutations in genes associated with ciliopathies. Ciliopathies are a group of genetic disorders that affect the structure and function of cilia, which are tiny hair-like structures found on the surface of cells. Cilia play a crucial role in various biological processes, including sensory perception, cell signaling, and fluid movement.

The Ciliopathies Panel NGS Genetic DNA Test utilizes advanced next-generation sequencing (NGS) technology to analyze multiple genes associated with ciliopathies. By identifying mutations in these genes, the test can help diagnose ciliopathy disorders such as Bardet-Biedl syndrome, Joubert syndrome, and nephronophthisis.

Healthcare providers typically order the Ciliopathies Panel NGS Genetic DNA Test for patients who exhibit symptoms and have a medical history suggestive of ciliopathy disorders. The test aids in confirming a diagnosis, guiding treatment decisions, and providing information about the risk of passing the condition on to future generations.

The Ciliopathies Panel NGS Genetic DNA Test is performed using a sample of the patient’s blood or saliva. The DNA is extracted and sequenced using NGS technology, and the results are carefully analyzed by genetic counselors or medical geneticists to interpret the findings.

If the Ciliopathies Panel NGS Genetic DNA Test is ordered by a healthcare provider and deemed medically necessary, it is typically covered by insurance.

Don’t let the symptoms of ciliopathies go undiagnosed. Contact DNA Labs UAE today to learn more about the Ciliopathies Panel NGS Genetic DNA Test and take the first step towards a clearer understanding of your genetic health.

 

Test Name Ciliopathies Panel NGS Genetic DNA Test
Components  
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for Ciliopathies Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACVR2B, AGPS, AHI1, ALPL, ANKH, ANO5, ARHGAP31, ARL13B, ARL6, ARMC4, ARSL, ATR, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BMP1, BMPR1B, C8ORF37, CANT1, CASR, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC28B, CCDC39, CCDC40, CCDC65, CCNO, CDKN1C, CENPF, CENPJ, CEP152, CEP164, CEP290, CEP41, CEP63, CFAP298, CFAP53, CFC1, CHSY1, CILK1, CLCN5, COL10A1, COL9A3, COMP, CPLANE1, CRELD1, CRTAP, CSPP1, DDR2, DHCR7, DMP1, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, DRC1, DYM, DYNC2H1, EBP, EIF2AK3, ENPP1, ESCO2, EVC, EVC2, FGF23, FKBP10, FLNB, GDF1, GDF5, GLI2, GLI3, GNAS, GNPAT, HEXA, HSPG2, HYDIN, HYLS1, IFITM5, IFT122, IFT140, IFT172, IFT27, IFT43, IFT80, INPP5E, INPPL1, KIF7, LBR, LEFTY2, LEP, LEPR, LIFR, LRP5, LRRC6, LZTFL1, MATN3, MKKS, MKS1, MMP13, MMP21, MMP9, MYO7A, NEK1, NEK8, NKX2-5, NKX3-2, NME8, NODAL, NOG, NPHP1, NPHP3, NR0B2, NSDHL, OFD1, P3H1, PDE6D, PEX7, PHEX, PHF6, PKD1L1, PKD2, PKHD1, PLOD2, PMM2, PNPLA6, POMC, PPARG, PPIB, PRKAR1A, PROM1, PRPH2, PTH1R, RBBP8, RDH5, RHO, RLBP1, ROR2, RPGRIP1L, RSPH1, RSPH4A, RSPH9, RUNX2, SALL1, SALL4, SBDS, SDCCAG8, SERPINF1, SERPINH1, SLC26A2, SLC34A3, SLC35D1, SOX9, SPAG1, TBX5, TCTN1, TCTN2, TCTN3, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TNFRSF11B, TRIM32, TRIP11, TRPS1, TRPV4, TTC21B, TTC8, WDPCP, WDR19, WDR34, WDR35, WDR60, WNT5A, WNT7A, ZIC3, ZMYND10, ZNF423
Test Details

The Ciliopathies Panel NGS Genetic DNA Test is a genetic test that analyzes the DNA of an individual for mutations in genes associated with ciliopathies. Ciliopathies are a group of genetic disorders that affect the structure and function of cilia, which are tiny hair-like structures found on the surface of cells. Cilia play an important role in many biological processes, including sensory perception, cell signaling, and fluid movement.

The Ciliopathies Panel NGS Genetic DNA Test uses next-generation sequencing (NGS) technology to analyze multiple genes associated with ciliopathies. The test can identify mutations that may cause or contribute to ciliopathy disorders such as Bardet-Biedl syndrome, Joubert syndrome, and nephronophthisis.

The test is typically ordered by a healthcare provider if a patient is suspected to have a ciliopathy disorder based on their symptoms and medical history. The test can help confirm a diagnosis, guide treatment decisions, and provide information about the risk of passing the condition on to future generations.

The Ciliopathies Panel NGS Genetic DNA Test is performed on a sample of the patient’s blood or saliva. The DNA is extracted and sequenced using NGS technology, and the results are analyzed by a genetic counselor or medical geneticist to interpret the findings. The test is typically covered by insurance if ordered by a healthcare provider and deemed medically necessary.
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