{"id":9648,"date":"2015-10-19T04:23:53","date_gmt":"2015-10-19T04:23:53","guid":{"rendered":"http:\/\/www.fetaldna.it\/home\/"},"modified":"2024-12-02T17:01:24","modified_gmt":"2024-12-02T17:01:24","slug":"home-2","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/en\/","title":{"rendered":"HOME"},"content":{"rendered":"

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FetalDNA:
\nNEXT-GENERATION
\nPRENATAL TEST<\/h1>

A cutting-edge technology
\nthat overcomes all the previous NIPTs<\/p>LEARN MORE<\/a><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>[\/vc_column][\/vc_row][vc_row equal_height=”yes” content_placement=”middle” softing_row_prepad=”ptb-30″ el_id=”livelli”][vc_column][vc_custom_heading text=”Explore FetalDNA Test” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_custom_heading text=”An innovative, reliable and safe, 100% made in Italy.
\nFor a peaceful pregnancy.” font_container=”tag:h3|text_align:center” use_theme_fonts=”yes”][vc_row_inner][vc_column_inner width=”1\/4″][vc_column_text]FetalDNA<\/strong> is a Non-Invasive Prenatal Test (NIPT)<\/strong> that allows to perform a complete genetic screening thanks to the circulating fetal DNA (= fragments of fetal DNA circulating in the maternal blood).<\/p>\n

With a simple blood sample from the pregnant woman, the Medical Genetics Laboratory of the Altamedica Healthcare Center in Rome<\/strong> can detect chromosomal abnormalities, microdeletions \/ microduplications and any other genetic diseases in the fetus as well as in the mother.<\/p>\n

The FetalDNA<\/strong> can be performed starting from the 10th week<\/strong>, for every kind of pregnancy<\/strong>\u00a0 (natural and obtained with assisted fertilization techniques).[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”3\/4″][vc_video link=”https:\/\/youtu.be\/bi7cXAetSvo”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row full_width=”stretch_row” equal_height=”yes” content_placement=”middle” softing_row_prepad=”ptb-30″ css=”.vc_custom_1640003788089{background-color: #dcdcdc !important;}”][vc_column][vc_custom_heading text=”FETALDNA SCREENING LEVELS” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

The fetal fetaldna day test before the investigation levels,
\nwith an increasing degree of approval:<\/span><\/h3>\n

[\/vc_column_text][vc_row_inner equal_height=”yes” softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”BASE” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”custom” i_background_style=”rounded” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Fnipt-mini-inipt%2F|title:FetalDNA%20Base|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Fnipt-mini-inipt%2F|title:FetalDNA%20Base|target:_blank” i_custom_color=”#eedbda”]It analyzes the most frequent trisomies with extreme precision:
\n21 (Down syndrome<\/strong>)
\n18 (Edwards syndrome<\/strong>)
\n13 (Patau syndrome<\/strong>)
\nGender of the child upon request<\/em>[\/vc_cta][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”BASE PLUS” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”custom” i_background_style=”rounded” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-base-plus-2%2F|title:FetalDNA%20Base%20Plus|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-base-plus-2%2F|title:FetalDNA%20Base%20Plus|target:_blank” i_custom_color=”#e4bbb7″]It integrates the BASE level (21, 18, 13) with investigation on abnormalities in the sex chromosomes X, Y<\/strong> (Turner syndrome, Klinefelter syndrome, etc.).<\/p>\n

Gender of the child upon request<\/em>[\/vc_cta][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”BASE PLUS + 90 MICRODELETIONS” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”custom” i_background_style=”rounded” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-base-plus-2%2F|title:FetalDNA%20Base%20Plus%20%2B21%20microdelezioni|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-base-plus-2%2F|title:FetalDNA%20Base%20Plus%20%2B21%20microdelezioni|target:_blank” i_custom_color=”#dc9e9c”]It adds 90 microdeletion \/ microduplication syndromes<\/strong> to BASE PLUS level (21<\/strong>, 18<\/strong>, 13<\/strong>, X<\/strong>, Y<\/strong>)<\/p>\n

Gender of the child upon request<\/em>[\/vc_cta][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”KARYOTYPE” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”custom” i_background_style=”rounded” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-cariotipo%2F|title:FetalDNA%20Cariotipo|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-cariotipo%2F|title:FetalDNA%20Cariotipo|target:_blank” i_custom_color=”#e18a7f”]It analyzes numerical alterations on all the 23 pairs of chromosomes<\/strong> of the fetus (including 13<\/strong>, 18<\/strong>, 21<\/strong> and sex chromosomes X and Y<\/strong>).<\/p>\n

Gender of the child upon request.<\/em>[\/vc_cta][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row full_width=”stretch_row” equal_height=”yes” content_placement=”middle” css=”.vc_custom_1640003633036{background-color: #dcdcdc !important;}”][vc_column width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”KARYOTYPE PLUS” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”custom” i_background_style=”rounded” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-cariotipo-plus%2F|title:FetalDNA%20Cariotipo%20Plus|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-cariotipo-plus%2F|title:FetalDNA%20Cariotipo%20Plus|target:_blank” i_custom_color=”#e5655a”]It integrates the previous level (fetal chromosomes aneuploidies<\/strong>), with the investigation on 90 chromosomal alterations from structural rearrangements<\/strong> (microduplications<\/strong> \/ microdeletions<\/strong>) as well as for the mutations related to Maternal Cystic Fibrosis<\/strong>.<\/p>\n

Gender of the child upon request.<\/em>[\/vc_cta][\/vc_column][vc_column width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”KARYOTYPE PLUS + MONOGENIC DISEASES” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”custom” i_background_style=”rounded” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-cariotipo-plus%2F|title:FetalDNA%20Cariotipo%20Plus%20%2B%20Monogeniche|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-cariotipo-plus%2F|title:FetalDNA%20Cariotipo%20Plus%20%2B%20Monogeniche|target:_blank” i_custom_color=”#e25047″]It adds the investigation on fetal monogenic diseases<\/strong> (caused by mutations of a single gene<\/strong>) such as beta thalassemia, congenital deafness, achondroplasia, fetal cystic fibrosis, etc., to the previous level (fetal karyotype, microdeletion \/ microduplication syndromes, maternal cystic fibrosis<\/strong>).<\/p>\n

Gender of the child upon request.<\/em>[\/vc_cta][\/vc_column][vc_column width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”TOTALSCREEN” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”custom” i_background_style=”rounded” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-total-screen%2F|title:FetalDNA%20Monogeniche|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldna.it%2Ffetaldna-total-screen%2F|title:FetalDNA%20Total%20Screen|target:_blank” i_custom_color=”#c54040″]It combines fetus and mother analysis<\/strong> for a peaceful pregnancy<\/strong>, adding further investigations to the previous level: risk of preterm birth, Maternal Spinal Muscular Atrophy (SMA), Hereditary Maternal Thrombophilia,<\/strong> risk of preeclampsia <\/strong>and infectious disease (cytomegalovirus and toxoplasmosis).<\/strong><\/p>\n

Gender of the child upon request.<\/em>[\/vc_cta][\/vc_column][vc_column width=”1\/4″][vc_cta h2=”FetalDNA” h2_font_container=”tag:h6|text_align:left” h2_use_theme_fonts=”yes” h4=”MONOGENIC DISEASES” color=”juicy-pink” add_button=”bottom” btn_title=”Learn more” btn_color=”juicy-pink” btn_i_icon_fontawesome=”fas fa-arrow-alt-circle-right” add_icon=”top” i_icon_fontawesome=”fas fa-circle” i_color=”white” i_background_style=”rounded” i_background_color=”custom” i_size=”lg” use_custom_fonts_h2=”true” btn_add_icon=”true” i_on_border=”true” h2_link=”url:https%3A%2F%2Fwww.fetaldnatotalscreen.it%2Fil-test-fetaldna%2F%23malattiemonogeniche|title:FetalDNA%20Cariotipo%20Plus%20%2B%20Monogeniche|target:_blank” btn_link=”url:https%3A%2F%2Fwww.fetaldnatotalscreen.it%2Fil-test-fetaldna%2F%23malattiemonogeniche|title:FetalDNA%20Cariotipo%20Plus%20%2B%20Monogeniche|target:_blank” css=”.vc_custom_1645999370455{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;border-left-color: #f2483e !important;border-left-style: dotted !important;border-right-color: #f2483e !important;border-right-style: dotted !important;border-top-color: #f2483e !important;border-top-style: dotted !important;border-bottom-color: #f2483e !important;border-bottom-style: dotted !important;}” i_custom_background_color=”#f2483e”]It explores the most important fetal monogenic diseases<\/strong>*<\/strong> (beta thalassemia, congenital deafness, achondroplasia, fetal cystic fibrosis, hemochromatosis, phenylketonuria, etc.)<\/p>\n

* It can be performed as a single request or in combination with the previous levels.<\/em><\/p>\n

Gender of the child upon request.<\/em>[\/vc_cta][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column width=”1\/6″][\/vc_column][vc_column width=”2\/3″][vc_custom_heading text=”Why choose FetalDNA Test” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][\/vc_column][vc_column width=”1\/6″][\/vc_column][\/vc_row][vc_row full_width=”stretch_row” equal_height=”yes” content_placement=”middle” parallax=”content-moving” parallax_image=”7358″][vc_column width=”1\/2″][vc_row_inner softing_row_prepad=”ptb-20″][vc_column_inner width=”1\/2″]

<\/i> <\/div>

SAFE<\/h4>

It is not traumatic for the mother nor the fetus and is completely free of abortion risks.<\/strong><\/p><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/2″]

<\/i> <\/div>

SIMPLE<\/h4>

A blood sample from mother\u2019s arm<\/strong> is enough for the analysis of circulating fetal DNA.<\/p><\/div><\/div>[\/vc_column_inner][\/vc_row_inner][vc_row_inner softing_row_prepad=”ptb-20″][vc_column_inner width=”1\/2″]

<\/i> <\/div>

FAST<\/h4>

Results are available within 5 working days <\/strong>(8 for the Total Screen) starting from the arrival of the sample at the Molecular Genetics laboratory.<\/p><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/2″]

<\/i> <\/div>

ACCURATE<\/h4>

High sensitivity and reliability of the test (99.9% for the main aneuploidies).<\/p><\/div><\/div>[\/vc_column_inner][\/vc_row_inner][vc_row_inner softing_row_prepad=”ptb-20″][vc_column_inner width=”1\/2″]

<\/i> <\/div>

STATE-OF-THE-ART<\/h4>

FetalDNA is developed by Altamedica specialists and it is analyzed completely in Italy with a patented technology<\/strong>.<\/p><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/2″]

<\/i> <\/div>

EASY TO UNDERSTAND<\/h4>

NEGATIVE:<\/strong> no anomalies
\nPOSITIVE:<\/strong> specific anomalies are indicated in the report<\/p><\/div><\/div>[\/vc_column_inner][\/vc_row_inner][\/vc_column][vc_column width=”1\/2″][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-50″][vc_column][vc_custom_heading text=”THREE SIMPLE STEPS” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/3″][vc_custom_heading text=”1. CHOOSE YOUR LEVEL” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes” css=”.vc_custom_1645998882349{border-bottom-width: 2px !important;border-bottom-color: #f2483e !important;border-bottom-style: dotted !important;}”][vc_column_text]Get a quick look at our materials (brochures<\/a>, consents<\/a>\u2026)<\/p>\n

You can book a free genetic counselling<\/strong> by filling this form<\/a>[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”2. BLOOD SAMPLE” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes” css=”.vc_custom_1645999601434{border-bottom-width: 2px !important;border-bottom-color: #f2483e !important;border-bottom-style: dotted !important;}”][vc_column_text css=”.vc_custom_1645999037528{margin-bottom: 2px !important;}”]Perform blood sampling at our Main Centers in Rome and Milan<\/strong>, in Altamedica partner centers<\/a>, with your doctor or at home. Before making the samplingl, you will be asked to fill in the forms for informed consent<\/a>.[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”3. RECEIVE THE RESULTS” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes” css=”.vc_custom_1645999054221{border-bottom-width: 2px !important;border-bottom-color: #f2483e !important;border-bottom-style: dotted !important;}”][vc_column_text css=”.vc_custom_1645999074302{margin-bottom: 2px !important;}”]You will receive the test results within 5 working days<\/strong> (8 only for FetalDNA Total Screen).<\/p>\n

In specific cases, you can request an emergency diagnostic service.[\/vc_column_text][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row full_width=”stretch_row_content” parallax=”content-moving” parallax_image=”13148″ softing_row_prepad=”ptb-60″ softing_row_overlay_type=”custom” softing_bg_attachment=”fixed” softing_lg_bgpos=”center” css=”.vc_custom_1641569817214{background-color: #f2483e !important;background-position: center;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_column parallax=”content-moving” parallax_image=”13154″ width=”1\/12″][\/vc_column][vc_column width=”3\/6″][\/vc_column][vc_column width=”2\/6″][vc_custom_heading text=”BOOK A FREE GENETIC COUNSELLING” font_container=”tag:h2|text_align:center|color:%23ffffff” use_theme_fonts=”yes” css=”.vc_custom_1645999120565{background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_custom_heading text=”Fill out the contact form to book an appointment with one of our Genetics Experts.
\nAll fields marked with an asterisk (*) are required.” font_container=”tag:p|text_align:left|color:%23ffffff” use_theme_fonts=”yes” css=”.vc_custom_1645999145685{background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”]\n

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