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FRAGILE X MUTATION (O.S.)

MRP: ₹10532

Recommended For

MaleFemale
  • Age Group
    0-99 Years
  • Report Generation Time
    09-Jun-2023 11:17 PM
  • Sample Type
    EDTA Blood
  • Collection At
    HomeLab
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Description

Mutations in the FMR1 gene cause fragile X syndrome. Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. This test is used to determine the number of time the CGG triplet is repeated to diagnose Fragile X syndrome.

Pre-Information

Duly filled Genomics Clinical Information Requisition Formis mandatory.

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    1 Test Included

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    1 Test Included

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    Add

  • IMMATURE PLATELET FRACTION (IPF)
    1 Test Included

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    1 Test Included

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    1 Test Included

    ₹500

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  • CATHACHOLAMINE ADRENALINE + NORADRENALINE (PLASMA) O.S.
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    1 Test Included

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    1 Test Included

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