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Ciliopathies Panel NGS Genetic DNA Test Cost 20000 Rs
Ciliopathies Panel NGS Genetic DNA Test Details
List of genes tested using NGS technology for detection of variant and mutation in Ciliopathies Panel are 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
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
Ciliopathies Panel NGS Genetic DNA Test
Cost: INR 20,000
What are Ciliopathies?
Ciliopathies are a group of genetic disorders that affect the structure or function of cilia, which are tiny, hair-like structures that line the surface of cells. These disorders can affect many different parts of the body, including the eyes, ears, kidneys, and respiratory system.
What is the Ciliopathies Panel NGS Genetic DNA Test?
The Ciliopathies Panel NGS Genetic DNA Test is a comprehensive genetic test that can help diagnose ciliopathies. This test uses Next Generation Sequencing (NGS) technology to analyze DNA samples and identify mutations in genes that are associated with ciliopathies.
What are the symptoms of Ciliopathies?
The symptoms of ciliopathies can vary depending on the specific disorder and which parts of the body are affected. Some common symptoms include:
- Vision problems
- Hearing loss
- Kidney problems
- Lung problems
- Skeletal abnormalities
How is Ciliopathies Panel NGS Genetic DNA Test performed?
The Ciliopathies Panel NGS Genetic DNA Test is a simple blood or saliva test. A small sample of blood or saliva is collected from the patient and sent to a laboratory for analysis. The laboratory will use NGS technology to sequence the patient's DNA and identify any mutations in genes associated with ciliopathies.
Why is the Ciliopathies Panel NGS Genetic DNA Test important?
The Ciliopathies Panel NGS Genetic DNA Test is important because it can help diagnose ciliopathies, which are often difficult to diagnose based on symptoms alone. Early diagnosis can lead to earlier treatment and better outcomes for patients.
Where can I get the Ciliopathies Panel NGS Genetic DNA Test?
The Ciliopathies Panel NGS Genetic DNA Test is available at DNA Labs India. To get tested, you can visit our website and order the test online. Once you have ordered the test, we will send you a sample collection kit that you can use to collect your blood or saliva sample. You can then send the sample back to us and we will analyze it in our state-of-the-art laboratory.
Conclusion:
The Ciliopathies Panel NGS Genetic DNA Test is a powerful tool for diagnosing ciliopathies, which are a group of genetic disorders that affect many different parts of the body. If you or a loved one are experiencing symptoms of ciliopathies, it is important to get tested as early as possible. With the Ciliopathies Panel NGS Genetic DNA Test, you can get an accurate diagnosis and start treatment sooner, which can lead to better outcomes.
