[et_pb_section fb_built=”1″ admin_label=”Section” module_class=”default-hero-section” _builder_version=”4.16.1″ _module_preset=”default” background_image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/geneticlab_about_header-min.png” da_disable_devices=”off|off|off” locked=”off” global_colors_info=”{}” da_is_popup=”off” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Section” module_class=”no-pt after-default-hero-section nipt” _builder_version=”4.17.3″ _module_preset=”default” da_disable_devices=”off|off|off” locked=”off” global_colors_info=”{}” da_is_popup=”off” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][et_pb_row column_structure=”2_5,3_5″ use_custom_gutter=”on” gutter_width=”1″ make_equal=”on” module_class=”border-radius box-shadow px5 py5 bg-white” _builder_version=”4.16.1″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”2_5″ module_class=”align-vert px6″ _builder_version=”4.16.1″ _module_preset=”default” global_colors_info=”{}”][et_pb_text module_class=”pb6″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

What is the<\/span> Non-Invasive Prenatal Test (NIPT)?<\/h1>\n

[\/et_pb_text][et_pb_text module_class=”mb4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

NIPT (Non-Invasive Prenatal Test) is a genetic screening test that a pregnant woman can perform from the 10th week of pregnancy. The NIPT test can determine if your baby has trisomy 21, trisomy 18, or trisomy 13. The term “trisomy” is used to describe the presence of an extra chromosome – or three instead of the usual pair.<\/p>\n

For example, trisomy 21 (Down syndrome) occurs when a baby is born with three children on chromosome 21. NIPT also provides additional testing options for certain other rare trisomies, sex chromosome aneuploids (an abnormal number of sex chromosomes) and changes in the number of children, which include deletion syndromes (a loss of part of a chromosome), duplication syndromes (an addition of part of a chromosome), and certain inherited genetic disorders (a disorder caused by a gene mutation that is transmitted from parent to child). If you want to know, the NIPT test can also provide information about the sex of the fetus.<\/p>\n

[\/et_pb_text][et_pb_button button_url=”\/wp-content\/uploads\/2022\/04\/geneticlab_brosura_teste_paternitate.pdf” url_new_window=”on” button_text=”Descarca flyer-ul Genetic Lab” disabled_on=”on|on|on” module_class=”primary-button dwld full” _builder_version=”4.17.3″ _module_preset=”default” disabled=”on” global_colors_info=”{}”][\/et_pb_button][\/et_pb_column][et_pb_column type=”3_5″ _builder_version=”4.16.1″ _module_preset=”default” background_image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/geneticlab_paternitate_intro-min.png” global_colors_info=”{}”][et_pb_image src=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/geneticlab_paternitate_intro-min.png” alt=”geneticlab_about_discover-min” title_text=”geneticlab_paternitate_intro-min” force_fullwidth=”on” disabled_on=”on|on|on” _builder_version=”4.16.1″ _module_preset=”default” disabled=”on” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Section” module_class=”mb5″ _builder_version=”4.16.1″ _module_preset=”default” da_disable_devices=”off|off|off” locked=”off” global_colors_info=”{}” da_is_popup=”off” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][et_pb_row module_class=”mw1460″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ module_class=”special-mobile-spacing” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

What are the benefits of<\/span> NIPT testing?<\/h2>\n

[\/et_pb_text][et_pb_text _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]NIPT testing is ideal for people who want to obtain information about the health of the fetus in a non-invasive way or to detect possible genetic abnormalities early in its development. The benefits of non-invasive testing include:[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_4,1_4,1_4,1_4″ use_custom_gutter=”on” gutter_width=”2″ make_equal=”on” module_class=”mw1460 spec-blurbs-row” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Elimination of the risk of miscarriage after consultation<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Detection of chromosomal disorders on 23 pairs of chromosomes<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Eligible health insurance – in case of positive screening tests<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Avoid an invasive diagnostic procedure<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_4,1_4,1_4,1_4″ use_custom_gutter=”on” gutter_width=”2″ make_equal=”on” module_class=”mw1460 spec-blurbs-row” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Accurate diagnosis of Down syndrome cases<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Obtaining accurate information on the health of the fetus<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Early detection of ultrasound abnormalities (any possible monogenic disorders)<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb image=”https:\/\/testepaternitate.ro\/wp-content\/uploads\/2022\/04\/check_icon.svg” icon_placement=”left” module_class=”spec-blurb” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Screening options for 96 different genetic conditions<\/h5>\n

[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Section” module_class=”mt6″ _builder_version=”4.17.3″ _module_preset=”default” da_disable_devices=”off|off|off” locked=”off” global_colors_info=”{}” da_is_popup=”off” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][et_pb_row use_custom_gutter=”on” gutter_width=”1″ module_class=”mw750″ _builder_version=”4.17.3″ _module_preset=”default” hover_enabled=”0″ global_colors_info=”{}” sticky_enabled=”0″][et_pb_column type=”4_4″ _builder_version=”4.17.3″ _module_preset=”default” hover_enabled=”0″ global_colors_info=”{}” sticky_enabled=”0″][et_pb_text _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Types of NIPT tests available<\/h2>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Section” module_class=”tests-listing-section nipt” _builder_version=”4.17.3″ _module_preset=”default” da_disable_devices=”off|off|off” locked=”off” global_colors_info=”{}” da_is_popup=”off” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][et_pb_row column_structure=”1_2,1_2″ use_custom_gutter=”on” gutter_width=”1″ make_equal=”on” module_class=”tests-listing-row” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.16.1″ _module_preset=”default” global_colors_info=”{}”][et_pb_text module_class=”test-listing__header px2″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

NIPT<\/h2>\n

for Trisomies 21, 18, 13, 9, 16, 22 + 84 Microdeletion\/Duplication Syndromes + Sex Chromosome Aneuploidy + with\/whitout Sex Information + Incidental findings*<\/p>\n

[\/et_pb_text][et_pb_text module_class=”test-listing__spec” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]This type of testing offers a clear and early conclusion regarding sex chromosomal aneuploidies or deletion\/duplication syndromes.[\/et_pb_text][et_pb_text module_class=”test-listing__spec explore” _builder_version=”4.17.3″ _module_preset=”default” link_option_url=”#nipt-popup1″ global_colors_info=”{}”]<\/p>\n

Explore the complete list of studied disorders<\/p>\n

[\/et_pb_text][et_pb_text module_class=”test-listing__spec” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]Free worldwide shipping and sample collection<\/span>[\/et_pb_text][et_pb_text module_class=”test-listing__spec” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]Results delivery duration<\/span> 10<\/b> days<\/span>[\/et_pb_text][et_pb_wc_price product=”895″ module_class=”test-listing__price” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_wc_price][et_pb_wc_add_to_cart product=”895″ show_quantity=”off” show_stock=”off” module_class=”test-listing__main” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_wc_add_to_cart][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.16.1″ _module_preset=”default” global_colors_info=”{}”][et_pb_text module_class=”test-listing__header” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

NIPT<\/h2>\n

for Non-invasive dominant single gene fetal screening<\/p>\n

[\/et_pb_text][et_pb_text module_class=”test-listing__spec” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]This test provides screening for 27 diseases, including skeletal, cardiac, and syndromic disorders caused by (2038) single-gene variants in 18 genes. The conditions examined include those associated with the average paternal age (men over the age of 40).[\/et_pb_text][et_pb_text module_class=”test-listing__spec explore” _builder_version=”4.17.3″ _module_preset=”default” link_option_url=”#nipt-popup2″ global_colors_info=”{}”]<\/p>\n

Explore the complete list of studied disorders<\/p>\n

[\/et_pb_text][et_pb_text module_class=”test-listing__spec” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]Free worldwide shipping and sample collection<\/span>[\/et_pb_text][et_pb_text module_class=”test-listing__spec” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]Results delivery duration<\/span> 16<\/b> days<\/span>[\/et_pb_text][et_pb_wc_price product=”894″ module_class=”test-listing__price” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_wc_price][et_pb_wc_add_to_cart product=”894″ show_quantity=”off” show_stock=”off” module_class=”test-listing__main” _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_wc_add_to_cart][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Section” _builder_version=”4.17.3″ _module_preset=”default” da_disable_devices=”off|off|off” locked=”off” global_colors_info=”{}” da_is_popup=”off” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][et_pb_row module_class=”mw1460″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.16.1″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

How does<\/span> NIPT work?<\/h2>\n

[\/et_pb_text][et_pb_text _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

During pregnancy, DNA from the mother and placenta circulates in the mother’s blood. NIPT works by taking a small sample of maternal blood of about 10ml and evaluating the genetic information in this sample. The assessment is done by applying whole-genome sequencing and advanced bioinformatics analysis to determine the risk of specific genetic disorders.<\/p>\n

NIPT is a screening test, which means that it does not test with 100% accuracy and, therefore should not be used as the sole basis for diagnosis or other pregnancy management decisions.[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Popup – #nipt-popup1″ module_id=”nipt-popup1″ module_class=”nipt-popup popup” _builder_version=”4.17.3″ _module_preset=”default” da_is_popup=”on” da_popup_slug=”nipt-popup1″ da_disable_devices=”off|off|off” global_colors_info=”{}” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][et_pb_row _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Trisomies<\/p>\n

\n
• Trisomy 21 (Down Syndrome)<\/li>\n
• Trisomy 18 (Edwards Syndrome)<\/li>\n
• Trisomy 13 (Patau Syndrome)<\/li>\n
• Trisomy 22<\/li>\n
• Trisomy 16<\/li>\n
• Trisomy9<\/li>\n
• Genetic sex identification<\/li>\n<\/ul>\n

  Sex chromosomal aneuploidies<\/p>\n

  \n
  • XXV (Klinefelter Syndrome)<\/li>\n
  • Monosomie X (Turner Syndrome)<\/li>\n
  • XXX (Triple X Syndrome)<\/li>\n
  • XYY(Jacob Syndrome)<\/li>\n<\/ul>\n

    Monosome Deletion \/ Duplication Syndromes<\/p>\n

    \n
    • Sp (Cri-du-Chat Syndrome)<\/li>\n
    • Prader-Willi \/ Angelman Syndrome (15q11.2)<\/li>\n
    • Jacobsen Syndrome (11q23)<\/li>\n
    • DiGeorge Syndrome<\/li>\n
    • DiGeorge II Syndrome (10p14-p13)<\/li>\n
    • Van der Woude Syndrome (1q32.2)<\/li>\n
    • Wolf-Hirschhorn Syndrome<\/li>\n
    • Miller-Dieker Syndrome<\/li>\n
    • Williams Beuren Syndrome<\/li>\n
    • Smith-Magenis Syndrome<\/li>\n
    • Dandy-Walker Syndrome<\/li>\n
    • Levy-Shansk Syndrome<\/li>\n
    • Split-hand \/fo ot malformation 5<\/li>\n
    • Holoprosencephaly 1, 6<\/li>\n
    • WAGRO Syndrome<\/li>\n
    • Yuan-Harel-Lupski Syndrome<\/li>\n
    • Cat-Eye Syndrome<\/li>\n
    • Langer-Giedion Syndrome<\/li>\n
    • Frias Syndrome<\/li>\n
    • CHDM<\/li>\n
    • WAGR Syndrome<\/li>\n
    • Potocki-Shaffe Syndrome<\/li>\n
    • HCD<\/li>\n
    • Potocki-Lupski Syndrome<\/li>\n
    • + other 57 diseases not specified here but just as important<\/li>\n<\/ul>\n

      [\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Popup – #nipt-popup2″ module_id=”nipt-popup2″ module_class=”nipt-popup popup” _builder_version=”4.17.3″ _module_preset=”default” da_is_popup=”on” da_popup_slug=”nipt-popup2″ da_disable_devices=”off|off|off” global_colors_info=”{}” da_exit_intent=”off” da_has_close=”on” da_alt_close=”off” da_dark_close=”off” da_not_modal=”on” da_is_singular=”off” da_with_loader=”off” da_has_shadow=”on”][et_pb_row _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.17.3″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

      Studied diseases<\/p>\n

      \n
      • Thanatophoric dysplasia, type I – Gene: FGFR3 – NO. of Variants: 5<\/li>\n
      • Thanatophoric dysplasia, type II – Gene: FGFR3 – NO. of Variants: 1<\/li>\n
      • Cardiofaciocutaneous syndrome IV – Gene: MAP2K2 – NO. of Variants: 4<\/li>\n
      • Cardiofaciocutaneous syndrome III – Gene: MAP2K1 – NO. of Variants: 4<\/li>\n
      • Cardiofaciocutaneous syndrome II – Gene: KRAS – NO. of Variants: 10<\/li>\n
      • Cardiofaciocutaneous syndrome – Gene: BRAF – NO. of Variants: 33<\/li>\n
      • Achondroplasia – Gene: FGFR3 – NO. of Variants: 6<\/li>\n
      • Campomelic dysplasia with autosomal sex Reversal – Gene: SOX9 – NO. of Variants: 19<\/li>\n
      • Acampomelic campomelic dysplasia – Gene: SOX9 – NO. of Variants: 18<\/li>\n
      • Acampomelic campomelic dysplasia – Gene: SOX9 – NO. of Variants: 18<\/li>\n
      • Tuberous sclerosis II – Gene: TSC2 – NO. of Variants: 476<\/li>\n
      • Tuberous sclerosis I – Gene: TSC1 – NO. of Variants: 176<\/li>\n
      • Osteogenesis imperfecta, type I – Gene: COL1A1 – NO. of Variants: 312<\/li>\n
      • Osteogenesis imperfecta, type II – Gene: COL1A1 – NO. of Variants: 32<\/li>\n
      • Osteogenesis imperfecta, type III – Gene: COL1A1 – NO. of Variants: 45<\/li>\n
      • Osteogenesis imperfecta, type IV – Gene: COL1A1 – NO. of Variants: 48<\/li>\n
      • Osteogenesis imperfecta, type I – Gene: COL1A2 – NO. of Variants: 18<\/li>\n
      • Osteogenesis imperfecta, type II – Gene: COL1A2 – NO. of Variants: 9<\/li>\n
      • Osteogenesis imperfecta, type III – Gene: COL1A2 – NO. of Variants: 12<\/li>\n
      • Osteogenesis imperfecta, type IV – Gene: COL1A2 – NO. of Variants: 19<\/li>\n
      • Osteogenesis imperfecta, type IV – Gene:COL1A2 – NO. of Variants:19<\/li>\n
      • Stickler syndrome, type I – Gene: COL2A1 – NO. of Variants:157<\/li>\n
      • Stickler syndrome, type II – Gene: COL11A1 – NO. of Variants: 17<\/li>\n
      • Pfeiffer syndrome – Gene: FGFR2 – NO. of Variants: 8<\/li>\n
      • Pfeiffer syndrome – Gene: FGFR1 – NO. of Variants: 1<\/li>\n
      • Jackson-Weiss syndrome – Gene: FGFR2 – NO. of Variants: 2<\/li>\n
      • Hutchinson-Gilford progeria – Gene: LMNA – NO. of Variants: 1<\/li>\n
      • Crouzon syndrome with acanthosis nigricans – Gene: FGFR3 – NO. of Variants:1<\/li>\n
      • Crouzon syndrome – Gene: FGFR2 – NO. of Variants: 19<\/li>\n
      • Costello syndrome – Gene: HRAS – NO. of Variants: 4<\/li>\n
      • CHARGE syndrome – Gene: CHD7 – NO. of Variants: 560<\/li>\n
      • Apert syndrome -Gene: FGFR2 – NO. of Variants:2<\/li>\n<\/ul>\n

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        What is the Non-Invasive Prenatal Test (NIPT)?NIPT (Non-Invasive Prenatal Test) is a genetic screening test that a pregnant woman can perform from the 10th week of pregnancy. The NIPT test can determine if your baby has trisomy 21, trisomy 18, or trisomy 13. The term “trisomy” is used to describe the presence of an extra […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-887","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/pages\/887","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/comments?post=887"}],"version-history":[{"count":13,"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/pages\/887\/revisions"}],"predecessor-version":[{"id":909,"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/pages\/887\/revisions\/909"}],"wp:attachment":[{"href":"https:\/\/testepaternitate.ro\/en\/wp-json\/wp\/v2\/media?parent=887"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}