{"id":9744,"date":"2015-10-19T04:23:53","date_gmt":"2015-10-19T04:23:53","guid":{"rendered":"http:\/\/www.fetaldna.it\/home\/"},"modified":"2024-12-02T16:59:53","modified_gmt":"2024-12-02T16:59:53","slug":"home-2","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/","title":{"rendered":"HOME"},"content":{"rendered":"

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FETALDNA:
\nTEST PR\u00c9NATAL NOUVELLE G\u00c9N\u00c9RATION<\/h1>

Une technologie de pointe qui surmonte tous les NIPT pr\u00e9c\u00e9dents
\nEn savoir plus<\/p>Plus d'information<\/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=”Explorez FetalDNA” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_custom_heading text=”Un test innovant, fiable et s\u00fbr, 100% made in Italy.
\nPour une grossesse sereine.” 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> est un Test Pr\u00e9natal Non Invasif (NIPT)<\/strong> qui permet d’effectuer un screening g\u00e9n\u00e9tique complet gr\u00e2ce \u00e0 l’ADN f\u0153tal circulant (= fragments d‘ADN f\u0153tal<\/strong> circulant dans le sang maternel).<\/p>\n

Avec un simple \u00e9chantillon de sang de la femme enceinte, le Laboratoire de G\u00e9n\u00e9tique M\u00e9dicale du Centre de Sant\u00e9 Altamedica \u00e0 Rome<\/strong> peut d\u00e9tecter des anomalies chromosomiques, des microd\u00e9l\u00e9tions \/ microduplications et toute autre maladie g\u00e9n\u00e9tique chez le f\u0153tus ainsi que chez la m\u00e8re.<\/p>\n

Le FetalDNA<\/strong> peut \u00eatre r\u00e9alis\u00e9 \u00e0 partir de la 10e semaine, pour tout type de grossesse<\/strong> (naturelle et obtenue avec des techniques de f\u00e9condation assist\u00e9e).[\/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=”NIVEAUX DE SCREENING DE FETALDNA” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

Le test du ADN foetal FetalDNA comprend 7 niveaux d’investigation, avec un degr\u00e9 croissant de profondeur:<\/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=”Plus d’information” 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”]Il analyse les trisomies les plus fr\u00e9quentes avec une extr\u00eame pr\u00e9cision :
\n21 (syndrome de Down<\/strong>)
\n18 (syndrome d’Edward<\/strong>)
\n13 (syndrome de Patau<\/strong>)<\/p>\n

Sexe de l’enfant sur demande<\/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=”Plus d’information” 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″]Il int\u00e8gre le niveau BASE (21, 18, 13) avec une recherche sur les anomalies des chromosomes sexuels X, Y<\/strong> (syndrome de Turner, syndrome de Klinefelter, etc.).<\/p>\n

Sexe de l’enfant sur demande<\/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=”Plus d’information” 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”]Il ajoute 90 syndromes de microd\u00e9l\u00e9tion\/microduplication<\/strong> au niveau BASE PLUS (21, 18, 13, X, Y)<\/p>\n

Sexe de l’enfant sur demande<\/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=”CARYOTYPE” color=”juicy-pink” add_button=”bottom” btn_title=”Plus d’information” 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”]Il analyse les alt\u00e9rations num\u00e9riques sur l’ensemble des 23 paires de chromosomes du f\u0153tus<\/strong> (dont 13, 18, 21 et les chromosomes sexuels X et Y).<\/p>\n

Sexe de l’enfant sur demande<\/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=”CARYOTYPE PLUS” color=”juicy-pink” add_button=”bottom” btn_title=”Plus d’information” 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”]Il int\u00e8gre le niveau pr\u00e9c\u00e9dent (aneuplo\u00efdies chromosomiques f\u0153tales<\/strong>), avec l’investigation de 90 alt\u00e9rations chromosomiques issues de r\u00e9arrangements structuraux<\/strong> (microduplications\/microd\u00e9l\u00e9tions<\/strong>) ainsi que pour les mutations li\u00e9es \u00e0 la Fibrose Kystique Maternelle<\/strong>.<\/p>\n

Sexe de l’enfant sur demande.<\/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=”CARYOTYPE PLUS + MALADIES MONOG\u00c8NES” color=”juicy-pink” add_button=”bottom” btn_title=”Plus d’information” 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″]Il ajoute l’investigation sur les maladies monog\u00e9niques f\u0153tales<\/strong> (caus\u00e9es par des mutations d’un seul g\u00e8ne<\/strong>) telles que la b\u00eata-thalass\u00e9mie<\/strong>, la surdit\u00e9 cong\u00e9nitale<\/strong>, l’achondroplasie<\/strong>, la mucoviscidose f\u0153tale<\/strong>, etc., au niveau pr\u00e9c\u00e9dent (caryotype f\u0153tal<\/strong>, syndromes de microd\u00e9l\u00e9tion<\/strong>\/microduplication<\/strong>, Fibrose Kystique Maternelle<\/strong>).<\/p>\n

Sexe de l’enfant sur demande.<\/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=”\u00c9CRAN TOTAL” color=”juicy-pink” add_button=”bottom” btn_title=”Plus d’information” 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″]Il combine l’analyse du f\u0153tus et de la m\u00e8re pour une grossesse sereine<\/strong>, ajoutant des investigations suppl\u00e9mentaires au niveau pr\u00e9c\u00e9dent: risque d’accouchement pr\u00e9matur\u00e9<\/strong>, amyotrophie spinale maternelle (SMA)<\/strong>, thrombophilie maternelle h\u00e9r\u00e9ditaire<\/strong>, risque de pr\u00e9\u00e9clampsie<\/strong> et de maladies infectieuses (cytom\u00e9galovirus et toxoplasmose<\/strong>).<\/p>\n

Sexe de l’enfant sur demande.<\/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=”MALADIES MONOG\u00c9NIQUES” color=”juicy-pink” add_button=”bottom” btn_title=”Plus d’information” 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_1665998773505{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”]Il explore les principales maladies monog\u00e9niques f\u0153tales<\/strong>* (b\u00eata-thalass\u00e9mie, surdit\u00e9 cong\u00e9nitale, achondroplasie, fibrose kystique maternelle, h\u00e9mochromatose, ph\u00e9nylc\u00e9tonurie, etc.)<\/p>\n

* On peut effectuer cette analyse en une seule demande ou en combinaison avec les niveaux pr\u00e9c\u00e9dents.<\/em><\/p>\n

Sexe de l’enfant sur demande.<\/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=”POURQUOI CHOISIR LE TEST FETALDNA” 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″]

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S\u00dbR<\/h4>

Il n'est traumatisant ni pour la m\u00e8re ni pour le f\u0153tus et ne present aucun risque <\/strong>d'avortement.<\/p><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/2″]

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FACILE<\/h4>

Un \u00e9chantillon de sang du bras<\/strong> de la m\u00e8re suffit pour l'analyse de l'ADN f\u0153tal circulant.<\/p><\/div><\/div>[\/vc_column_inner][\/vc_row_inner][vc_row_inner softing_row_prepad=”ptb-20″][vc_column_inner width=”1\/2″]

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RAPIDE<\/h4>

Les r\u00e9sultats sont disponibles dans 5 jours ouvrables<\/strong> (8 pour l\u2019\u00c9cran Total) \u00e0 compter de la reception de l'\u00e9chantillon par le Laboratoire de G\u00e9n\u00e9tique Mol\u00e9culaire.<\/p><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/2″]

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PR\u00c9CIS<\/h4>

Haute sensibilit\u00e9 <\/strong> et fiabilit\u00e9<\/strong> du test (99,9% pour les principales aneuplo\u00efdies).<\/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>

AVANT-GARDE<\/h4>

FetalDNA est d\u00e9velopp\u00e9 par les sp\u00e9cialistes d'Altamedica et est enti\u00e8rement analys\u00e9 en Italie avec une technologie brevet\u00e9e<\/strong>.<\/p><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/2″]

<\/i> <\/div>

FACILE \u00c0 COMPRENDRE<\/h4>

N\u00c9GATIF<\/strong> : aucune anomalie
\nPOSITIF<\/strong> : des anomalies sp\u00e9cifiques sont signal\u00e9es dans le rapport<\/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=”TROIS \u00c9TAPES SIMPLES” 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 CHOISISSEZ
\nVOTRE NIVEAU” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes” css=”.vc_custom_1647296097247{border-bottom-width: 2px !important;border-bottom-color: #f2483e !important;border-bottom-style: dotted !important;}”][vc_column_text]D\u00e9couvrez rapidement nos supports (brochures<\/a>, consentements<\/a>\u2026)<\/p>\n

Vous pouvez r\u00e9server un conseil g\u00e9n\u00e9tique gratuit en remplissant ce formulaire<\/a>[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”2 PR\u00c9LEVEZ
\nL’\u00c9CHANTILLON DE SANG” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes” css=”.vc_custom_1647361347841{border-bottom-width: 2px !important;border-bottom-color: #f2483e !important;border-bottom-style: dotted !important;}”][vc_column_text css=”.vc_custom_1647296244672{margin-bottom: 2px !important;}”]Effectuez des pr\u00e9l\u00e8vements de sang dans nos centres principaux de Rome et de Milan<\/strong>, dans les centres partenaires d’Altamedica<\/a>, avec votre m\u00e9decin ou \u00e0 domicile. Avant de proc\u00e9der au pr\u00e9l\u00e8vement, il vous sera demand\u00e9 de remplir les formulaires<\/strong> de consentement \u00e9clair\u00e9<\/a>.[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”3 RECEVOIR
\nLES R\u00c9SULTATS” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes” css=”.vc_custom_1647296259145{border-bottom-width: 2px !important;border-bottom-color: #f2483e !important;border-bottom-style: dotted !important;}”][vc_column_text css=”.vc_custom_1647296305277{margin-bottom: 2px !important;}”]Vous recevrez les r\u00e9sultats du test dans 5 jours ouvrables<\/strong> (8<\/strong> uniquement pour FetalDNA \u00c9cran Total<\/strong>).<\/p>\n

Dans des cas sp\u00e9cifiques, vous pouvez demander un service de diagnostic d’urgence.[\/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=”R\u00c9SERVER UN CONSEIL G\u00c9N\u00c9TIQUE GRATUIT” font_container=”tag:h2|text_align:center|color:%23ffffff” use_theme_fonts=”yes” css=”.vc_custom_1647296318680{background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_custom_heading text=”Remplissez le formulaire de contact pour prendre rendez-vous avec l’un de nos Experts en G\u00e9n\u00e9tique.
\nTous les champs marqu\u00e9s d’un ast\u00e9risque (*) sont obligatoires.” font_container=”tag:p|text_align:left|color:%23ffffff” use_theme_fonts=”yes” css=”.vc_custom_1647296345153{background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”]\n

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