{"id":9731,"date":"2017-08-02T16:40:08","date_gmt":"2017-08-02T16:40:08","guid":{"rendered":"http:\/\/www.fetaldna.it\/basic-fetaldna\/"},"modified":"2024-12-16T12:58:57","modified_gmt":"2024-12-16T12:58:57","slug":"basic-fetaldna","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/","title":{"rendered":"FetalDNA Basic"},"content":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641815422294{padding-top: 100px !important;padding-bottom: 50px !important;background-image: url(https:\/\/www.fetaldna.it\/wp-content\/uploads\/2019\/04\/header_mom.jpg?id=10022) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_column css=”.vc_custom_1641815492985{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_custom_heading text=”FetalDNA Basic” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

The FetalDNA Base level investigates the most common chromosomal abnormalities (aneuploidies).<\/h3>\n

[\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/3″][vc_custom_heading text=”Down syndrome” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646168898634{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][vc_column_text]<\/p>\n

Trisomy of chromosome 21<\/strong><\/p>\n

It is one of the most common aneuploidy; it refers to the presence of an extra copy of chromosome 21.<\/p>\n

[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Edwards syndrome” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646168947471{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][vc_column_text]<\/p>\n

Trisomy of chromosome 18<\/strong><\/p>\n

Presence of an extra copy of chromosome 18.<\/p>\n

[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Patau syndrome” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646168994134{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][vc_column_text]<\/p>\n

Trisomy of chromosome 13<\/strong><\/p>\n

Presence of an extra copy of chromosome 13.<\/p>\n

[\/vc_column_text][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=”” full_width=”stretch_row”][vc_column 0=””][vc_separator color=”custom” border_width=”2″ accent_color=”#f2483e”][vc_column_text css=”.vc_custom_1671729123082{padding-top: 5% !important;}”]FetalDNA Base<\/strong> investigates the main anomalies in numbers of chromosomes (aneuploidies<\/em>): the term Trisomy<\/em> means that, for that particular chromosome, 3 copies are observed instead of 2, while the term Monosomy<\/em> means that particular chromosome is observed as a single copy instead of 2.<\/p>\n

The FetalDna Base<\/strong> level specifically investigates the anomalies of chromosome 21<\/strong> (Down syndrome<\/strong>), chromosome 18<\/strong> (Edward syndrome<\/strong>) and chromosome 13<\/strong> (Patau syndrome<\/strong>), it represents the overcoming of the traditional combined tests included in the first trimester screenings (e.g. Bi-test, Tri-test, etc.)<\/p>\n

It is the test recommended by all the Guidelines and by the Scientific Societies; according to the official indications of the Ministry of Health, the FetalDNA BASE<\/strong> prenatal test must be added to the ultrasound study of nuchal translucency.<\/p>\n

This examination has extremely low costs for the patient and a high response speed.<\/strong><\/p>\n

Fetal sex can also be provided upon request but NOT sex chromosomal abnormalities.<\/em>[\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/4″][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_btn title=”BOOK A FREE GENETIC COUNSELLING” style=”effect” size=”lg” softing_vc_btn_brdstyle=”solid” link=”url:tel%3A068505800|target:_blank” softing_vc_btn_title=”#ffffff” softing_vc_btn_bg=”#f2483e” softing_vc_btn_hvrtitle=”#f2483e” softing_vc_btn_brdclr=”#f2483e” softing_vc_btn_hvrbrdclr=”#f2483e” softing_vc_btn_hvrbg=”#ffffff”][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner][vc_message message_box_color=”grey”]<\/p>\n

Results are available within 5 working days (but time may increase in case of technical difficulties during DNA analysis or if patient needs to repeat the test).<\/h4>\n

The prenatal test carries out a sophisticated and reliable screening but not a diagnosis, regardless of the company and the technology used. Diagnostic certainty is provided only by invasive tests (Amniocentesis and CVS) as reported in all the guidelines and international scientific literature.<\/h4>\n

In the event that the DNA screening test (FetalDNA Base) reveals abnormalities, the Altamedica Healthcare Center offers free confirmation tests through prenatal diagnosis (CVS or Amniocentesis), within our Healthcare Center in Rome.<\/h4>\n

[\/vc_message][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=”” full_width=”stretch_row_content” softing_row_prepad=”ptb-30″ css=”.vc_custom_1641403975693{background-color: rgba(242,72,62,0.41) !important;*background-color: rgb(242,72,62) !important;}”][vc_column 0=””][vc_custom_heading text=”In order to investigate other chromosomal and genetic alterations, it is suggested to choose more advanced NIPT tests:” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes”][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/6″]

<\/i> <\/div>

<\/p>\n

FETALDNA BASE PLUS<\/h4>\n

<\/h4><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/6″]

<\/i> <\/div>

<\/p>\n

FETALDNA BASE PLUS + 90 MICRODELEZIONI<\/h4>\n

<\/h4><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/6″]

<\/i> <\/div>

<\/p>\n

FETALDNA CARIOTIPO<\/h4>\n

<\/h4><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/6″]

<\/i> <\/div>

<\/p>\n

FETALDNA CARIOTIPO PLUS<\/h4>\n

<\/h4><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/6″]

<\/i> <\/div>

<\/p>\n

FETALDNA TOTAL SCREEN<\/h4>\n

<\/h4><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/6″]

<\/i> <\/div>

<\/p>\n

MALATTIE MONOGENICHE<\/h4>\n

<\/h4><\/div><\/div>[\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=”” full_width=”stretch_row_content” css=”.vc_custom_1641403916348{padding-top: 3% !important;padding-bottom: 3% !important;}”][vc_column 0=””][vc_custom_heading text=”Table comparison” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes”][vc_single_image source=”external_link” external_img_size=”small” alignment=”center” custom_src=”https:\/\/www.fetaldna.it\/img\/01_ComparativeTable_FetalDNA_Basic_EN.png”][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641815422294{padding-top: 100px !important;padding-bottom: 50px !important;background-image: url(https:\/\/www.fetaldna.it\/wp-content\/uploads\/2019\/04\/header_mom.jpg?id=10022) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_column css=”.vc_custom_1641815492985{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_custom_heading text=”FetalDNA Basic” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text] The FetalDNA Base level investigates the most common chromosomal abnormalities (aneuploidies). [\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/3″][vc_custom_heading text=”Down syndrome” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646168898634{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top:…<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"custom-page.php","meta":{"footnotes":""},"class_list":["post-9731","page","type-page","status-publish","hentry"," c-blog-1-item nt-post-class"],"yoast_head":"\nNIPT - FetalDNA Base - mini iNIPT - Altamedica Roma<\/title>\n<meta name=\"description\" content=\"Test NIPT base per individuare le 3 principali trisomie (cromosoma 13, 18 e 21). Esame da aggiungere alla translucenza nucale.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"NIPT - FetalDNA Base - mini iNIPT - Altamedica Roma\" \/>\n<meta property=\"og:description\" content=\"Test NIPT base per individuare le 3 principali trisomie (cromosoma 13, 18 e 21). Esame da aggiungere alla translucenza nucale.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/\" \/>\n<meta property=\"og:site_name\" content=\"FetalDNA\" \/>\n<meta property=\"article:modified_time\" content=\"2024-12-16T12:58:57+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"4 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/en\\\/basic-fetaldna\\\/\",\"url\":\"https:\\\/\\\/www.fetaldna.it\\\/en\\\/basic-fetaldna\\\/\",\"name\":\"NIPT - FetalDNA Base - mini iNIPT - Altamedica Roma\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/#website\"},\"datePublished\":\"2017-08-02T16:40:08+00:00\",\"dateModified\":\"2024-12-16T12:58:57+00:00\",\"description\":\"Test NIPT base per individuare le 3 principali trisomie (cromosoma 13, 18 e 21). Esame da aggiungere alla translucenza nucale.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/en\\\/basic-fetaldna\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.fetaldna.it\\\/en\\\/basic-fetaldna\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/en\\\/basic-fetaldna\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.fetaldna.it\\\/en\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"FetalDNA Basic\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/#website\",\"url\":\"https:\\\/\\\/www.fetaldna.it\\\/\",\"name\":\"FetalDNA | Il test prenatale su DNA fetale\",\"description\":\"Il test prenatale di ultima generazione\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.fetaldna.it\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"NIPT - FetalDNA Base - mini iNIPT - Altamedica Roma","description":"Test NIPT base per individuare le 3 principali trisomie (cromosoma 13, 18 e 21). Esame da aggiungere alla translucenza nucale.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/","og_locale":"en_US","og_type":"article","og_title":"NIPT - FetalDNA Base - mini iNIPT - Altamedica Roma","og_description":"Test NIPT base per individuare le 3 principali trisomie (cromosoma 13, 18 e 21). Esame da aggiungere alla translucenza nucale.","og_url":"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/","og_site_name":"FetalDNA","article_modified_time":"2024-12-16T12:58:57+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"4 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/","url":"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/","name":"NIPT - FetalDNA Base - mini iNIPT - Altamedica Roma","isPartOf":{"@id":"https:\/\/www.fetaldna.it\/#website"},"datePublished":"2017-08-02T16:40:08+00:00","dateModified":"2024-12-16T12:58:57+00:00","description":"Test NIPT base per individuare le 3 principali trisomie (cromosoma 13, 18 e 21). Esame da aggiungere alla translucenza nucale.","breadcrumb":{"@id":"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.fetaldna.it\/en\/basic-fetaldna\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.fetaldna.it\/en\/"},{"@type":"ListItem","position":2,"name":"FetalDNA Basic"}]},{"@type":"WebSite","@id":"https:\/\/www.fetaldna.it\/#website","url":"https:\/\/www.fetaldna.it\/","name":"FetalDNA | Il test prenatale su DNA fetale","description":"Il test prenatale di ultima generazione","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.fetaldna.it\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"}]}},"_links":{"self":[{"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/pages\/9731","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/comments?post=9731"}],"version-history":[{"count":13,"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/pages\/9731\/revisions"}],"predecessor-version":[{"id":13887,"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/pages\/9731\/revisions\/13887"}],"wp:attachment":[{"href":"https:\/\/www.fetaldna.it\/en\/wp-json\/wp\/v2\/media?parent=9731"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}