పరిశోధన వివరాలు

  • అధ్యయనం గురించి

    Diabetic retinopathy is a sight-threatening complication of both type 1 and type 2 diabetes. Genetic factors account for 25-50% of the risk of developing diabetes retinopathy. In this study, evaluate the Indian population for genetic markers associated with diabetic retinopathy.

  • పాల్గొనడానికి ఎవరు అర్హులు

    Inclusion Criteria
    1. Patients of either sex, receiving a clinical diagnosis of diabetic retinopathy
    2. Patients of either sex, having Diabetes Mellitus but not having diabetic retinopathy
    3. Patients aged 18 years and above, and consenting for research study as per the attached Informed Consent
    4. Population studied: Patients of Indian origin with both parents and all 4 grandparents born in India

    Exclusion Criteria
    1. Patients with any past history of eye trauma
    2. Patients diagnosed with diabetic retinopathy combined with congenital ocular disease or any other disease
    3. Patients diagnosed with or having a family history of neurodegenerative diseases

  • పాల్గొనేవారికి ప్రయోజనాలు

    Free Genomepatri Test along with Counseling worth Rs.7999.

నమోదు ముగింపు

Enroll Now

పరిమిత స్థలాలు అందుబాటులో ఉన్నాయి. 500 పాల్గొనేవారిని కోరుతున్నారు

తరచుగా అడుగు ప్రశ్నలు

HOW WILL I RECEIVE THE GENOMEPATRI KIT?

Genomepatri test kit can either be mailed to your postal address or
our technician will deliver the kit and collect the sample from your
home.

HOW IS THE SAMPLE COLLECTED?

Genomepatri’s sample collection kit has a buccal/saliva swab which
is used for collecting a saliva sample. It is very easy to use and the kit comes with printed instructions on how to do the sampling. After you complete the sampling, all you have to do is inform us and we will pick
it up for processing.

WHAT TECHNOLOGY IS USED FOR GENOMEPATRI?

Genomepatri uses a DNA sequencing technology called genotyping which is performed on microarrays.

HOW DO YOU DO THE ANALYSIS?

We screen your genetic data for the presence of “markers” in your DNA
- which are single letter variations - to calculate your lifestyle
disease risk, predisposition to traits, drug response, etc. We have
developed a robust algorithm which is used for analysis, based on
genetic markers present in your DNA sample. These single letter
variations are known as Single Nucleotide Polymorphisms or SNPs.

WHEN WILL I GET THE RESULTS?

The results will be ready after 3 weeks and a genetic counselor will
schedule a session to explain the results to you in the language of your choice.

ప్రచురణలు మరియు అన్వేషణలు