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01 About the test

By analyzing the whole genome through a SNP chromosomal microarray, bebegene® can screen for many rare diseases.

bebegene® is a screening test for 137 rare genetic diseases related to developmental disorders of newborn babies. It detects possible problems which can lead to early diagnosis and treatment and 5000+ variants screening for AR metabolic disorders, AR disorders, AD disorders and XLD.

02 Benefits

  • 01 Detects possible problems which can lead to
    early diagnosis and treatment

    02 Test options for Developmental disorders,
    Organ disorders and Physical disability

    03 Patient-friendly test reports

    04 Provide genetic counselling services for Doctor

03 bebegene® Series
- CNV & SNV related diseases

  • bebegene®
    (Lite)

    • deletions/
      duplications

  • bebegene®
    (Basic)

    • deletions/duplications
    • AR metabolic disorder, Wilson's, hearing loss, CFTR related

  • bebegene®
    (Premium)

    • deletions/duplications
    • AR metabolic disorder, Wilson's, hearing loss, CFTR related
    • 32- XLD and AD disorders eg Achondroplasia, Noonan syndrome, XL-Alport

04 How is the bebegene
performed

  • Test period

    From after birth

  • Specimen

    0.1ml of blood with EDTA or 0.5ml of cord blood

  • Turnaround time

    TAT 7-10 Working days

EDGCName of Representative : Min-Seob Lee

Tel : +82-32-713-2100

EDGC, Inc.#143, Gaetbeol-ro, Yeonsu-gu, Incheon, 21999, South Korea Tel : +1-800-605-8422

  • ⓒ[2022]. Eone Diagnomics Genome Center Co., Ltd. All Rights Reserved.
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