Short Description

List of genes tested using NGS technology for detection of variant and mutation in Intellectual disability panel are ABAT, ABCD1, ACE, ACSL4, ACTB, ACTG1, ACTN4, ADA, ADAR, ADCY5, ADGRG1, ADK, ADNP, ADSL, AFF2, AHI1, AIMP1, AKAP9, AKT3, ALDH18A1, ALDH5A1, ALDH7A1, ALG11, ALG13, ALX4, AMPD1, AMPD2, AMT, ANK2, ANK3, ANKRD11, AP1S1, AP1S2, AP3B1, AP4B1, AP4M1, ARFGEF2, ARHGEF10, ARHGEF6, ARHGEF9, ARID1A, ARID1B, ARL13B, ARX, ASAH1, ASCL1, ASPM, ASXL1, ASXL3, ATP13A2, ATP1A3, ATP6AP2, ATP6V0A2, ATP7A, ATP8A2, ATR, ATRX, AUTS2, B3GALNT2, B4GAT1, B9D1, B9D2, BBS4, BCAP31, BCKDK, BCOR, BCS1L, BDNF, BLOC1S3, BLOC1S6, BRAF, BRCA2, BRWD3, C12orf57, C12orf65, C19orf12, CA2, CA8, CACNA1A, CACNA1C, CACNA1D, CACNA1F, CACNA1H, CACNB2, CAMTA1, CARD11, CASK, CBS, CC2D1A, CC2D2A, CCDC40, CCDC88C, CDH15, CDK5RAP2, CDKL5, CDON, CENPF, CENPJ, CEP135, CEP152, CEP290, CEP41, CEP63, CHD2, CHD7, CHD8, CHMP1A, CHRM3, CIB2, CLCN4, CLIC2, CLN8, CNGB3, CNTNAP2, COASY, COL4A1, CPLANE1, CPT2, CRADD, CRBN, CREBBP, CRIPT, CRPPA, CSPP1, CTC1, CTNNA3, CTNNB1, CUL3, CUL4B, CUL7, CYB5R3, CYP11B1, CYP27A1, DARS2, DCAF17, DCX, DDC, DDX3X, DHCR7, DKC1, DLG3, DNM1, DOCK8, DPYD, DRD3, DST, DTNBP1, DYM, DYNC1H1, DYRK1A, EDN3, EDNRB, EEF1A2, EFTUD2, EHMT1, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF4E, ELOVL4, EMX2, EP300, EPB41L1, ESRRB, ETFB, EXOSC3, FAM126A, FANCB, FBN1, FGA, FGD1, FGFR2, FGFR3, FH, FKRP, FKTN, FLNA, FLVCR1, FMR1, FOLR1, FOXC1, FOXG1, FOXL2, FOXP1, FOXP2, FTL, FTO, FTSJ1, G6PD, GABRB3, GAD1, GAMT, GATM, GCK, GDI1, GDNF, GFAP, GIGYF2, GJC2, GK, GLI2, GLRB, GMPPA, GMPPB, GNAO1, GNAS, GPC3, GPHN, GPT2, GPX1, GRIA3, GRID2, GRIK2, GRIN1, GRIN2A, GRIN2B, GRIP1, HBB, HCCS, HCFC1, HCN1, HDAC4, HDAC8, HEPACAM, HERC2, HNRNPU, HOXA1, HPRT1, HPS1, HPS4, HPS5, HPS6, HRAS, HSD17B10, HSPD1, HUWE1, HYDIN, IDS, IER3IP1, IFIH1, IGBP1, IGF1, IGF1R, IL1RAPL1, INPP5E, INVS, IQSEC2, IRX5, ITGA7, ITGB3, ITPR1, JAG1, KANK1, KAT6A, KAT6B, KATNB1, KCNB1, KCNC1, KCNC3, KCND3, KCNJ10, KCNK9, KCNMA1, KCNQ2, KCNQ3, KDM5C, KDM6A, KIF11, KIF1A, KIF5C, KIF7, KIRREL3, KMT2A, KMT2C, KMT2D, KNL1, KRAS, L1CAM, LAMA1, LAMA2, LAMB1, LAMC3, LAMP2, LARGE1, LEP, LINS1, LMX1B, LRBA, LRP2, LZTR1, MAGEL2, MAGT1, MAN1B1, MAOA, MBD5, MBTPS2, MCCC2, MCM4, MCPH1, MECP2, MED12, MED13L, MED17, MED23, MEF2C, MEGF10, MEIS2, MET, MFRP, MFSD2A, MGAT2, MIB1, MID1, MITF, MKKS, MKS1, MLC1, MPDZ, MSMO1, MTHFR, MTM1, MTOR, MTR, MYCN, MYO5A, NAA10, NAGA, NALCN, NDE1, NDP, NDST1, NDUFA1, NECTIN1, NEXMIF, NF1, NFIX, NHEJ1, NHS, NIPA1, NIPBL, NLGN3, NLGN4X, NOTCH2, NPHP1, NPHP3, NR2F1, NR3C2, NRXN1, NSD1, NSDHL, NSUN2, NTRK1, NXF5, OCLN, OCRL, OFD1, OPHN1, ORC1, OTC, PAFAH1B1, PAH, PAK3, PANK2, PAX3, PAX6, PCDH15, PCDH19, PCNT, PDE6D, PDHA1, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PGAP1, PGK1, PHC1, PHF6, PHF8, PIGA, PIGL, PIGN, PIGO, PIGV, PIK3R2, PITX2, PLA2G6, PLCB1, PLK4, PLN, PLP1, PNKP, POGZ, POLR3A, POLR3B, POMGNT1, POMGNT2, POMK, POMT1, POMT2, PORCN, POT1, PPOX, PPT1, PQBP1, PRICKLE1, PRKN, PRODH, PRPS1, PRSS12, PTCH1, PTEN, PTPN11, PTPRC, PTS, PURA, PYCR1, PYCR2, QARS1, RAB18, RAB39B, RAB3GAP1, RAB3GAP2, RAD21, RAI1, RARS2, RBBP8, RBFOX1, RBM10, RELN, RET, RIMS1, RNASEH2A, RNASEH2B, RNASEH2C, ROGDI, ROR2, RPGRIP1L, RPL10, RPS6KA3, RXYLT1, SALL1, SAMHD1, SASS6, SATB2, SBF1, SCN1A, SCN2A, SCN4A, SCN8A, SCN9A, SCO2, SDCCAG8, SDHA, SEPSECS, SETBP1, SETD2, SGCA, SHANK2, SHH, SHROOM4, SIL1, SIX3, SLC12A5, SLC16A2, SLC25A12, SLC25A15, SLC25A19, SLC27A4, SLC2A1, SLC35A2, SLC35A3, SLC4A4, SLC6A1, SLC6A3, SLC6A8, SLC7A7, SLC9A6, SLC9A9, SLCO1B3, SMAD4, SMARCA2, SMARCA4, SMARCB1, SMARCE1, SMC1A, SMC3, SMPD1, SMS, SNAI2, SNAP29, SNIP1, SOBP, SOD1, SOX10, SOX2, SOX3, SPAST, SRD5A3, ST3GAL3, STAMBP, STIL, STRA6, STXBP1, SYN1, SYNE1, SYNGAP1, SYNJ1, SYP, TAF2, TAF6, TBC1D20, TBC1D24, TBCE, TBL1XR1, TBX1, TCF4, TCTN1, TCTN2, TCTN3, TECR, TECTA, TFAP2A, TGIF1, THRA, TIMM8A, TINF2, TMCO1, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TMLHE, TPO, TRAPPC9, TREX1, TRMT10A, TRPC6, TSC1, TSC2, TSEN2, TSEN34, TSEN54, TSPAN7, TTC21B, TTI2, TTN, TUBA1A, TUBA8, TUBB2B, TUBB3, TUBB4A, TUBGCP4, TUBGCP6, TUSC3, TYR, UBE2A, UBE3A, UBR1, UPF3B, USH2A, USP9X, VDR, VLDLR, VPS13B, VPS53, VRK1, WAC, WDR45, WDR62, WDR81, WNT1, WNT5A, WWOX, YWHAE, ZBTB18, ZDHHC9, ZEB2, ZFYVE26, ZIC2, ZIC3, ZNF335, ZNF41, ZNF423, ZNF711, ZNF81

PreTest Information

Clinical History of Patient who is going for Intellectual disability panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Intellectual disability panel

Detail Description

Intellectual Disability Panel NGS Genetic DNA Test Cost INR: 20000 Symptoms Diagnosis

Intellectual disability (ID) is a condition characterized by significant limitations in cognitive function and adaptive behavior. It affects 1-3% of the population globally and can be caused by genetic, environmental, or unknown factors. The Intellectual Disability Panel NGS Genetic DNA Test is a diagnostic tool that can help identify genetic causes of ID. In this blog, we will discuss the symptoms, diagnosis, and cost of this test.

Symptoms of Intellectual Disability

The symptoms of intellectual disability vary widely depending on the severity of the condition. Some common symptoms include:

• Delayed milestones such as sitting up, crawling, or walking
• Difficulty with communication and language
• Poor memory and problem-solving abilities
• Difficulty with social skills
• Behavioral problems such as aggression or hyperactivity
• Physical abnormalities such as small head size or facial features

Diagnosis of Intellectual Disability

Diagnosis of intellectual disability involves a comprehensive evaluation of the individual's cognitive function and adaptive behavior. This may include:

• Developmental assessments to measure skills and abilities
• Standardized tests to assess intelligence and adaptive behavior
• Medical tests to rule out other conditions that may cause similar symptoms
• Genetic testing to identify underlying genetic causes of ID

Intellectual Disability Panel NGS Genetic DNA Test

The Intellectual Disability Panel NGS Genetic DNA Test is a genetic test that uses next-generation sequencing (NGS) technology to identify genetic causes of ID. The test analyzes a panel of genes associated with ID and can detect mutations, deletions, and duplications in these genes. The test can be performed on a blood or saliva sample and typically takes 4-6 weeks for results.

Cost of Intellectual Disability Panel NGS Genetic DNA Test

The cost of the Intellectual Disability Panel NGS Genetic DNA Test in India is approximately INR 20,000. However, the cost may vary depending on the laboratory and additional tests that may be required. It is important to consult with a healthcare professional to determine the appropriate diagnostic testing for an individual with ID.

Conclusion

The Intellectual Disability Panel NGS Genetic DNA Test is a valuable diagnostic tool for identifying genetic causes of ID. The test can help healthcare professionals develop personalized treatment plans and provide families with information about the underlying cause of their child's condition. While the cost of the test may vary, it is a worthwhile investment in the health and well-being of individuals with ID.

At DNA Labs India, we offer a range of genetic testing services including the Intellectual Disability Panel NGS Genetic DNA Test. Contact us today to learn more about our services and how we can assist you.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for Intellectual disability panel NGS Genetic DNA Test