Nx Gen Sequencing Charcot-Marie-Tooth Disease and Sensory Neuropathies Test sale cost 4680 AED
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Nx Gen Sequencing Charcot-Marie-Tooth Disease and Sensory Neuropathies Test Cost

Original price was: 5,200 د.إ.Current price is: 4,680 د.إ.

-10%

The “Nx Gen Sequencing Charcot-Marie-Tooth Disease and Sensory Neuropathies Test” is an advanced diagnostic tool offered by DNA Labs UAE, designed to identify genetic mutations associated with Charcot-Marie-Tooth disease and other related sensory neuropathies. Utilizing next-generation sequencing technology, this comprehensive test can analyze multiple genes known to be linked with these conditions, providing valuable insights into the genetic underpinnings of an individual’s symptoms. With a cost of 4680 AED, the test aims to facilitate early diagnosis, guide treatment decisions, and offer prognostic information, ultimately contributing to improved patient care and management strategies for those affected by these debilitating neurological disorders.

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  • This test is not intended for medical diagnosis or treatment
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Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test

Welcome to DNA Labs UAE, where we offer advanced genetic testing services. One of our featured tests is the Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test. This test is designed to diagnose Charcot-Marie-Tooth Disease (CMT) and other sensory neuropathies.

Test Components

The Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test includes the following components:

  • AARS
  • ABHD12
  • AIFM1
  • ARHGEF10
  • ATL1
  • ATL3
  • ATP1A1
  • ATP7A
  • BAG3
  • BSCL2
  • CCT5
  • CNTNAP1
  • COA7
  • COX6A1
  • CTDP1
  • DCTN1
  • DCTN2
  • DHTKD1
  • DNAJB2
  • DNM2
  • DNMT1
  • DRP2
  • DST
  • DYNC1H1
  • EGR2
  • FAM134B
  • FGD4
  • FIG4
  • GAN
  • GARS
  • GDAP1
  • GJB1
  • GNB4
  • HARS
  • HINT1
  • HK1
  • HOXD1
  • HSPB1
  • HSPB3
  • HSPB8
  • IGHMBP2
  • INF2
  • JPH1
  • KARS
  • KIF1A
  • KIF1B
  • KIF5A
  • LITAF
  • LMNA
  • LRSAM1
  • MARS
  • MCM3AP
  • MED25
  • MFN2
  • MME
  • MORC2
  • MPV17
  • MPZ
  • MTMR2
  • NAGLU
  • NDRG1
  • NEFH
  • NEFL
  • NGF
  • NTRK1
  • PDK3
  • PLEKHG5
  • PMP22
  • PRDM12
  • PRPS1
  • PRX
  • PTRH2
  • RAB7A
  • SBF1
  • SBF2
  • SCN11A
  • SCO2
  • SCN9A
  • SETX
  • SGPL1
  • SH3TC2
  • SIGMAR1
  • SLC12A6
  • SLC25A46
  • SOX1
  • SPG11
  • SPTLC1
  • SPTLC2
  • SURF1
  • TFG
  • TRIM2
  • TRPV4
  • VCP
  • WARS
  • WNK1
  • YARS

Test Cost

The cost of the Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test is 4680.0 AED.

Symptoms and Diagnosis

Charcot-Marie-Tooth Disease (CMT) and sensory neuropathies are characterized by muscle weakness and sensory loss in the arms and legs. If you are experiencing these symptoms, it is important to consult a neurologist for a proper diagnosis.

Sample Condition

To perform the test, we require a sample of 10 mL (5 mL minimum) whole blood from 2 Lavender Top (EDTA) tubes. The sample should be shipped refrigerated and should not be frozen. Additionally, a duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.

Report Delivery

The sample should be submitted daily by 9 am. The report will be delivered within 40 working days.

Method

The Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test utilizes next-generation sequencing (NGS) and Sanger sequencing methods.

Test Type

The Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test falls under the category of Genetic Disorders-Hereditary Motor & Sensory Neuropathy.

Doctor

This test is typically recommended by neurologists.

Test Department

The Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test is conducted in our Molecular Diagnostics department.

Pre Test Information

Prior to the test, it is mandatory to fill out the Whole Exome Sequencing Consent Form (Form 37).

Test Details

The Nx Gen Sequencing test is a powerful next-generation sequencing (NGS) test used to diagnose Charcot-Marie-Tooth Disease (CMT) and other sensory neuropathies. CMT is a group of inherited disorders that affect the peripheral nerves, resulting in muscle weakness and sensory loss in the arms and legs.

By analyzing the patient’s DNA, the Nx Gen Sequencing test can identify mutations in genes associated with CMT and sensory neuropathies. This comprehensive analysis allows for the detection of mutations in multiple genes simultaneously, aiding in confirming a diagnosis of CMT and determining the specific subtype of the disease.

The test also provides valuable information about the prognosis and potential treatment options for the patient, enabling personalized and targeted approaches to managing Charcot-Marie-Tooth Disease and other sensory neuropathies.

Test Name Nx GEN SEQUENCING CHARCOT-MARIE-TOOTH DISEASE and SENSORY NEUROPATHIES Test
Components AARS, ABHD12, AIFM1, ARHGEF10, ATL1, ATL3, ATP1A1, ATP7A, BAG3, BSCL2, CCT5, CNTNAP1, COA7, COX6A1, CTDP1, DCTN1, DCTN2, DHTKD1, DNAJB2, DNM2, DNMT1, DRP2, DST, DYNC1H1, EGR2, FAM134B, FGD4, FIG4, GAN, GARS, GDAP1, GJB1, GNB4, HARS, HINT1, HK1, HOXD1, HSPB1, HSPB3, HSPB8, IGHMBP2, INF2, JPH1, KARS, KIF1A, KIF1B, KIF5A, LITAF, LMNA, LRSAM1, MARS, MCM3AP, MED25, MFN2, MME, MORC2, MPV17, MPZ, MTMR2, NAGLU, NDRG1, NEFH, NEFL, NGF, NTRK1, PDK3, PLEKHG5, PMP22, PRDM12, PRPS1, PRX, PTRH2, RAB7A, SBF1, SBF2, SCN11A, SCO2, SCN9A, SETX, SGPL1, SH3TC2, SIGMAR1, SLC12A6, SLC25A46, SOX1, SPG11, SPTLC1, SPTLC2, SURF1, TFG, TRIM2, TRPV4, VCP, WARS, WNK1, YARS
Price 4680.0 AED
Sample Condition Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE. Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Report Delivery Sample Daily by 9 am; Report 40 Working days
Method NGS, Sanger sequencing
Test type Genetic Disorders-Hereditary Motor & Sensory Neuropathy
Doctor Neurologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Test Details

Nx Gen Sequencing is a next-generation sequencing (NGS) test that is used to diagnose Charcot-Marie-Tooth Disease (CMT) and other sensory neuropathies. CMT is a group of inherited disorders that affect the peripheral nerves, causing muscle weakness and sensory loss in the arms and legs.

The Nx Gen Sequencing test analyzes the patient’s DNA to identify mutations in genes associated with CMT and sensory neuropathies. This test can detect mutations in multiple genes simultaneously, providing a comprehensive analysis of the patient’s genetic makeup.

By identifying specific gene mutations, the Nx Gen Sequencing test can help confirm a diagnosis of CMT and determine the subtype of the disease. It can also provide information about the prognosis and potential treatment options for the patient.

Overall, Nx Gen Sequencing is a powerful tool in the diagnosis and management of Charcot-Marie-Tooth Disease and other sensory neuropathies, allowing for personalized and targeted treatment approaches.

SKU: TEST-4623 Category:

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