Sale!

Dysmorphology Panel NGS Genetic Test Cost

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

-27%

The Dysmorphology Panel NGS (Next-Generation Sequencing) Genetic Test is a sophisticated diagnostic tool offered by DNA Labs UAE, designed to identify genetic mutations responsible for dysmorphic features and congenital anomalies. This comprehensive test utilizes cutting-edge NGS technology to analyze multiple genes simultaneously, making it highly efficient in pinpointing the genetic basis of various dysmorphological syndromes. With a test cost of 4400 AED, the panel aims to provide crucial insights into the genetic disorders affecting an individual’s physical appearance and structural development, facilitating early diagnosis and personalized management plans. DNA Labs UAE ensures precision, reliability, and confidentiality in delivering results, empowering healthcare professionals and families with essential genetic information to guide clinical decisions and support.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

Dysmorphology Panel NGS Genetic Test

Test Name: Dysmorphology 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 Dysmorphology Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with various genetic conditions.

Test Details

The Dysmorphology Panel NGS Genetic DNA Test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze a person’s DNA for mutations and variations that may be associated with physical abnormalities or developmental disorders.

Dysmorphology refers to the study of physical abnormalities or differences in body structure and appearance. These abnormalities can be caused by genetic mutations or environmental factors and can lead to developmental disorders such as intellectual disability, autism spectrum disorder, or congenital malformations.

The Dysmorphology Panel NGS Genetic DNA Test examines a panel of genes that are known to be associated with dysmorphology and developmental disorders. The test can identify mutations or variations in these genes that may contribute to a person’s physical abnormalities or developmental issues.

The test is typically ordered by a healthcare provider or genetic counselor when there is a suspicion of a genetic condition or developmental disorder. Results from the test can help with diagnosis, treatment, and management of the condition.

 

Test NameDysmorphology Panel NGS Genetic DNA Test
Components 
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeDysmorphology
DoctorPediatrics
Test Department:Genetics
Pre Test InformationClinical 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
Test Details

The Dysmorphology Panel NGS Genetic DNA Test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze a person’s DNA for mutations and variations that may be associated with physical abnormalities or developmental disorders.

Dysmorphology refers to the study of physical abnormalities or differences in body structure and appearance. These abnormalities can be caused by genetic mutations or environmental factors, and can lead to developmental disorders such as intellectual disability, autism spectrum disorder, or congenital malformations.

The Dysmorphology Panel NGS Genetic DNA Test examines a panel of genes that are known to be associated with dysmorphology and developmental disorders. The test can identify mutations or variations in these genes that may contribute to a person’s physical abnormalities or developmental issues.

The test is typically ordered by a healthcare provider or genetic counselor when there is a suspicion of a genetic condition or developmental disorder. Results from the test can help with diagnosis, treatment, and management of the condition.