Why to get tested at DNA Labs India for Dysmorphology Panel NGS Genetic DNA Test ?
Book Now
-
3500 Sample collection centers, Free Home Sample
collection for Dysmorphology Panel NGS Genetic DNA Test in your city
-
Ranked India No1 DNA Test Lab for
Dysmorphology Panel NGS Genetic DNA Test
-
Most Trusted Lab by doctors for Dysmorphology Panel NGS Genetic DNA Test. Call 07941057551 to talk with Doctor to
get second opinion for free of cost
-
Dysmorphology Panel NGS Genetic DNA Test Cost 20000 Rs
Dysmorphology Panel NGS Genetic DNA Test Details
List of genes tested using NGS technology for detection of variant and mutation in Dysmorphology Panel are ABCB6, ABCC6, ACTA1, ACTA2, ACTB, ACTG1, ACVR2B, ADAMTS2, ADAMTSL2, ADGRG1, AFF4, AGPS, AGRN, AHI1, AKT3, ALDH18A1, ALDH1A3, ALG2, ALPL, AMPD2, ANKH, ANKRD11, ANO5, AP4M1, ARFGEF2, ARHGAP31, ARID1A, ARID1B, ARL13B, ARL6, ARMC4, ARSL, ARX, ASPM, ASXL1, ASXL3, ATP6V0A2, ATP7A, ATR, ATRX, B3GALNT2, B3GALT6, B3GAT3, B4GALT7, B4GAT1, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCOR, BGN, BIN1, BMP1, BMP4, BMPR1B, BRAF, C8orf37, CANT1, CASK, CASR, CBL, CBS, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC28B, CCDC39, CCDC40, CCDC65, CCM2, CCNO, CDK5RAP2, CDKN1C, CDON, CENPF, CENPJ, CEP135, CEP152, CEP164, CEP290, CEP41, CEP63, CFAP298, CFAP53, CFC1, CFL2, CHAT, CHD7, CHMP1A, CHRNA1, CHRNB1, CHRND, CHRNE, CHRNG, CHST14, CHSY1, CILK1, CLCN5, COASY, COL10A1, COL11A1, COL11A2, COL12A1, COL1A1, COL1A2, COL2A1, COL3A1, COL4A1, COL5A1, COL5A2, COL6A1, COL6A2, COL6A3, COL9A1, COL9A2, COL9A3, COLQ, COMP, COX7B, CPLANE1, CREB3L1, CREBBP, CRELD1, CRIPT, CRPPA, CRTAP, CSPP1, CUL7, CYP1B1, DAG1, DCX, DDR2, DHCR24, DHCR7, DMP1, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, DNM2, DOK7, DPAGT1, DRC1, DSE, DYM, DYNC1H1, DYNC2H1, DYRK1A, EBP, ECE1, ECEL1, EDN3, EDNRB, EFEMP2, EFNB1, EFTUD2, EGR2, EIF2AK3, ELN, ENPP1, ERCC1, ERCC2, ERCC5, ERCC6, ERF, ESCO2, EVC, EVC2, EXOSC3, FAS, FBLN5, FBN1, FBN2, FGF23, FGF8, FGFR1, FGFR2, FGFR3, FHL1, FKBP10, FKBP14, FKRP, FKTN, FLCN, FLNA, FLNB, FOXC1, FOXE3, FOXH1, FOXL2, FRAS1, FREM1, FREM2, GBA, GBE1, GDF1, GDF3, GDF5, GDF6, GDNF, GFPT1, GJA1, GLE1, GLI2, GLI3, GMPPB, GNAS, GNPAT, GORAB, GRIP1, HCCS, HDAC8, HESX1, HEXA, HMGB3, HMX1, HRAS, HSPG2, HUWE1, HYDIN, HYLS1, IER3IP1, IFITM5, IFT122, IFT140, IFT172, IFT27, IFT43, IFT80, IL11RA, INPP5E, INPPL1, IRF6, ITGB4, KAT6B, KATNB1, KBTBD13, KDM5C, KDM6A, KIF11, KIF2A, KIF5C, KIF7, KIT, KLHL40, KLHL41, KMT2A, KMT2D, KNL1, KRAS, KRIT1, L1CAM, LAMA2, LAMA3, LAMB1, LAMB3, LAMC2, LARGE1, LBR, LEFTY2, LEP, LEPR, LIFR, LMNA, LMOD3, LMX1B, LOX, LRP2, LRP5, LRRC6, LZTFL1, LZTR1, MAB21L2, MAGEL2, MAP2K1, MAP2K2, MASP1, MAT2A, MATN3, MBTPS2, MCPH1, MED12, MED17, MEGF8, MEIS2, MEOX1, MFAP5, MFRP, MFSD2A, MITF, MKKS, MKS1, MMP13, MMP21, MMP9, MSMO1, MSX1, MSX2, MTM1, MUSK, MYBPC1, MYCN, MYH11, MYH2, MYH3, MYH8, MYLK, MYO18B, MYO7A, NAA10, NALCN, NDE1, NDP, NEB, NECTIN1, NEK1, NEK8, NF1, NF2, NHEJ1, NIPBL, NKX2-5, NKX3-2, NME8, NODAL, NOG, NOTCH1, NPHP1, NPHP3, NR0B2, NRAS, NRG1, NSDHL, OCRL, OFD1, ORC1, OTX2, P3H1, PAFAH1B1, PAX2, PAX3, PAX6, PCNT, PDCD10, PDE6D, PEX7, PHC1, PHEX, PHF6, PIEZO2, PIGV, PITX2, PKD1L1, PKD2, PKHD1, PLK4, PLOD1, PLOD2, PMM2, PNKP, PNPLA6, POMC, POMGNT1, POMGNT2, POMK, POMT1, POMT2, POR, PPARG, PPIB, PQBP1, PRDM5, PRKAR1A, PRKG1, PROM1, PRPH2, PRSS56, PTCH1, PTH1R, PTPN11, PYCR1, PYCR2, QARS1, RAB18, RAB23, RAB3GAP1, RAB3GAP2, RAD21, RAF1, RAPSN, RARB, RARS2, RASA1, RASA2, RAX, RBBP8, RBP4, RDH5, RELN, RET, RHO, RIN2, RIT1, RLBP1, ROR2, RPGRIP1L, RPL10, RPS6KA3, RSPH1, RSPH4A, RSPH9, RUNX2, RXYLT1, RYR1, SALL1, SALL2, SALL4, SASS6, SATB2, SBDS, SCN4A, SDCCAG8, SELENON, SEPSECS, SERPINF1, SERPINH1, SHH, SHOC2, SHROOM4, SIX3, SIX6, SKI, SLC25A19, SLC26A2, SLC2A10, SLC34A3, SLC35D1, SLC39A13, SLC5A7, SLC9A6, SMAD2, SMAD3, SMAD4, SMAD6, SMARCA2, SMARCA4, SMARCB1, SMARCE1, SMC1A, SMC3, SMCHD1, SMOC1, SNAI2, SOS1, SOS2, SOX10, SOX2, SOX9, SP7, SPAG1, SPRED1, STAMBP, STIL, STRA6, SUMO1, TAF6, TBC1D20, TBC1D24, TBX5, TCF12, TCF4, TCTN1, TCTN2, TCTN3, TENM3, TFAP2A, TGFB2, TGFB3, TGFBR1, TGFBR2, TGIF1, TK2, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TNFRSF11B, TNNI2, TNNT1, TNNT3, TNXB, TOR1A, TP63, TPM2, TPM3, TRIM32, TRIP11, TRMT10A, TRPS1, TRPV4, TSC1, TSC2, TSEN2, TSEN54, TTC21B, TTC8, TUBA1A, TUBA8, TUBB, TUBB2A, TUBB2B, TUBB3, TUBG1, TUBGCP4, TUBGCP6, TWIST1, TYR, UBA1, VAMP1, VIPAS39, VLDLR, VPS13B, VPS53, VRK1, VSX2, WDPCP, WDR19, WDR34, WDR35, WDR60, WDR62, WNT1, WNT5A, WNT7A, YWHAE, ZEB2, ZIC2, ZIC3, ZMYND10, ZNF335, ZNF423, ZNF469
Clinical History of Patient who is going for Dysmorphology Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABCB6, ABCC6, ACTA1, ACTA2, ACTB, ACTG1, ACVR2B, ADAMTS2, ADAMTSL2, ADGRG1, AFF4, AGPS, AGRN, AHI1, AKT3, ALDH18A1, ALDH1A3, ALG2, ALPL, AMPD2, ANKH, ANKRD11, ANO5, AP4M1, ARFGEF2, ARHGAP31, ARID1A, ARID1B, ARL13B, ARL6, ARMC4, ARSL, ARX, ASPM, ASXL1, ASXL3, ATP6V0A2, ATP7A, ATR, ATRX, B3GALNT2, B3GALT6, B3GAT3, B4GALT7, B4GAT1, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCOR, BGN, BIN1, BMP1, BMP4, BMPR1B, BRAF, C8orf37, CANT1, CASK, CASR, CBL, CBS, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC28B, CCDC39, CCDC40, CCDC65, CCM2, CCNO, CDK5RAP2, CDKN1C, CDON, CENPF, CENPJ, CEP135, CEP152, CEP164, CEP290, CEP41, CEP63, CFAP298, CFAP53, CFC1, CFL2, CHAT, CHD7, CHMP1A, CHRNA1, CHRNB1, CHRND, CHRNE, CHRNG, CHST14, CHSY1, CILK1, CLCN5, COASY, COL10A1, COL11A1, COL11A2, COL12A1, COL1A1, COL1A2, COL2A1, COL3A1, COL4A1, COL5A1, COL5A2, COL6A1, COL6A2, COL6A3, COL9A1, COL9A2, COL9A3, COLQ, COMP, COX7B, CPLANE1, CREB3L1, CREBBP, CRELD1, CRIPT, CRPPA, CRTAP, CSPP1, CUL7, CYP1B1, DAG1, DCX, DDR2, DHCR24, DHCR7, DMP1, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, DNM2, DOK7, DPAGT1, DRC1, DSE, DYM, DYNC1H1, DYNC2H1, DYRK1A, EBP, ECE1, ECEL1, EDN3, EDNRB, EFEMP2, EFNB1, EFTUD2, EGR2, EIF2AK3, ELN, ENPP1, ERCC1, ERCC2, ERCC5, ERCC6, ERF, ESCO2, EVC, EVC2, EXOSC3, FAS, FBLN5, FBN1, FBN2, FGF23, FGF8, FGFR1, FGFR2, FGFR3, FHL1, FKBP10, FKBP14, FKRP, FKTN, FLCN, FLNA, FLNB, FOXC1, FOXE3, FOXH1, FOXL2, FRAS1, FREM1, FREM2, GBA, GBE1, GDF1, GDF3, GDF5, GDF6, GDNF, GFPT1, GJA1, GLE1, GLI2, GLI3, GMPPB, GNAS, GNPAT, GORAB, GRIP1, HCCS, HDAC8, HESX1, HEXA, HMGB3, HMX1, HRAS, HSPG2, HUWE1, HYDIN, HYLS1, IER3IP1, IFITM5, IFT122, IFT140, IFT172, IFT27, IFT43, IFT80, IL11RA, INPP5E, INPPL1, IRF6, ITGB4, KAT6B, KATNB1, KBTBD13, KDM5C, KDM6A, KIF11, KIF2A, KIF5C, KIF7, KIT, KLHL40, KLHL41, KMT2A, KMT2D, KNL1, KRAS, KRIT1, L1CAM, LAMA2, LAMA3, LAMB1, LAMB3, LAMC2, LARGE1, LBR, LEFTY2, LEP, LEPR, LIFR, LMNA, LMOD3, LMX1B, LOX, LRP2, LRP5, LRRC6, LZTFL1, LZTR1, MAB21L2, MAGEL2, MAP2K1, MAP2K2, MASP1, MAT2A, MATN3, MBTPS2, MCPH1, MED12, MED17, MEGF8, MEIS2, MEOX1, MFAP5, MFRP, MFSD2A, MITF, MKKS, MKS1, MMP13, MMP21, MMP9, MSMO1, MSX1, MSX2, MTM1, MUSK, MYBPC1, MYCN, MYH11, MYH2, MYH3, MYH8, MYLK, MYO18B, MYO7A, NAA10, NALCN, NDE1, NDP, NEB, NECTIN1, NEK1, NEK8, NF1, NF2, NHEJ1, NIPBL, NKX2-5, NKX3-2, NME8, NODAL, NOG, NOTCH1, NPHP1, NPHP3, NR0B2, NRAS, NRG1, NSDHL, OCRL, OFD1, ORC1, OTX2, P3H1, PAFAH1B1, PAX2, PAX3, PAX6, PCNT, PDCD10, PDE6D, PEX7, PHC1, PHEX, PHF6, PIEZO2, PIGV, PITX2, PKD1L1, PKD2, PKHD1, PLK4, PLOD1, PLOD2, PMM2, PNKP, PNPLA6, POMC, POMGNT1, POMGNT2, POMK, POMT1, POMT2, POR, PPARG, PPIB, PQBP1, PRDM5, PRKAR1A, PRKG1, PROM1, PRPH2, PRSS56, PTCH1, PTH1R, PTPN11, PYCR1, PYCR2, QARS1, RAB18, RAB23, RAB3GAP1, RAB3GAP2, RAD21, RAF1, RAPSN, RARB, RARS2, RASA1, RASA2, RAX, RBBP8, RBP4, RDH5, RELN, RET, RHO, RIN2, RIT1, RLBP1, ROR2, RPGRIP1L, RPL10, RPS6KA3, RSPH1, RSPH4A, RSPH9, RUNX2, RXYLT1, RYR1, SALL1, SALL2, SALL4, SASS6, SATB2, SBDS, SCN4A, SDCCAG8, SELENON, SEPSECS, SERPINF1, SERPINH1, SHH, SHOC2, SHROOM4, SIX3, SIX6, SKI, SLC25A19, SLC26A2, SLC2A10, SLC34A3, SLC35D1, SLC39A13, SLC5A7, SLC9A6, SMAD2, SMAD3, SMAD4, SMAD6, SMARCA2, SMARCA4, SMARCB1, SMARCE1, SMC1A, SMC3, SMCHD1, SMOC1, SNAI2, SOS1, SOS2, SOX10, SOX2, SOX9, SP7, SPAG1, SPRED1, STAMBP, STIL, STRA6, SUMO1, TAF6, TBC1D20, TBC1D24, TBX5, TCF12, TCF4, TCTN1, TCTN2, TCTN3, TENM3, TFAP2A, TGFB2, TGFB3, TGFBR1, TGFBR2, TGIF1, TK2, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TNFRSF11B, TNNI2, TNNT1, TNNT3, TNXB, TOR1A, TP63, TPM2, TPM3, TRIM32, TRIP11, TRMT10A, TRPS1, TRPV4, TSC1, TSC2, TSEN2, TSEN54, TTC21B, TTC8, TUBA1A, TUBA8, TUBB, TUBB2A, TUBB2B, TUBB3, TUBG1, TUBGCP4, TUBGCP6, TWIST1, TYR, UBA1, VAMP1, VIPAS39, VLDLR, VPS13B, VPS53, VRK1, VSX2, WDPCP, WDR19, WDR34, WDR35, WDR60, WDR62, WNT1, WNT5A, WNT7A, YWHAE, ZEB2, ZIC2, ZIC3, ZMYND10, ZNF335, ZNF423, ZNF469
Dysmorphology Panel NGS Genetic DNA Test: A Comprehensive Guide
Are you concerned about your child's physical appearance? Do you suspect a genetic disorder that may be causing it? Dysmorphology Panel NGS Genetic DNA Test can help diagnose the symptoms. In this blog, we will discuss everything you need to know about the test, including cost, symptoms, and diagnosis.
What is Dysmorphology Panel NGS Genetic DNA Test?
Dysmorphology Panel NGS Genetic DNA Test is a genetic test that examines a patient's DNA to identify any genetic abnormalities that may cause physical abnormalities. This test specifically focuses on dysmorphology, the study of abnormal physical features.
The test is performed using Next Generation Sequencing (NGS) technology, which enables rapid and accurate testing of multiple genes simultaneously. The test can detect a wide range of genetic disorders that affect physical appearance and development.
What are the symptoms of genetic disorders detected by Dysmorphology Panel NGS Genetic DNA Test?
Genetic disorders that affect physical appearance can cause a wide range of symptoms, including:
- Abnormal facial features, such as a small head or widely spaced eyes
- Unusual skin pigmentation
- Abnormalities in limb or body size and shape
- Developmental delays or intellectual disability
- Abnormalities in internal organs, such as heart defects
If your child is experiencing any of these symptoms, it may be an indication of a genetic disorder, and a Dysmorphology Panel NGS Genetic DNA Test can help diagnose the cause.
How is Dysmorphology Panel NGS Genetic DNA Test performed?
The test is performed using a blood sample or a cheek swab. The DNA is extracted from the sample, and the NGS technology is used to sequence multiple genes simultaneously. The results are then analyzed by a geneticist to identify any genetic abnormalities that may be causing the symptoms.
What is the cost of Dysmorphology Panel NGS Genetic DNA Test?
The cost of the test can vary depending on the laboratory and location. At DNA Labs India, Dysmorphology Panel NGS Genetic DNA Test costs INR 20,000. It is important to note that insurance may cover some or all of the cost of the test.
How is Dysmorphology Panel NGS Genetic DNA Test helpful?
Dysmorphology Panel NGS Genetic DNA Test can help diagnose the cause of physical abnormalities and developmental delays, allowing for early intervention and treatment. Additionally, it can help identify the risk of genetic disorders in future pregnancies, allowing for informed family planning decisions.
Conclusion
Dysmorphology Panel NGS Genetic DNA Test is a comprehensive genetic test that can identify the cause of physical abnormalities and developmental delays. The test is performed using NGS technology, which allows for rapid and accurate testing of multiple genes simultaneously. The cost of the test may vary, but it is an important investment in the health and well-being of your child. If you suspect a genetic disorder, talk to your doctor about Dysmorphology Panel NGS Genetic DNA Test.
At DNA Labs India, we offer a wide range of genetic tests, including Dysmorphology Panel NGS Genetic DNA Test. Contact us today to schedule a consultation.
