{"id":9672,"date":"2018-04-18T16:38:14","date_gmt":"2018-04-18T16:38:14","guid":{"rendered":"http:\/\/www.fetaldna.it\/fetaldna-base-plus-2\/"},"modified":"2024-12-16T13:00:14","modified_gmt":"2024-12-16T13:00:14","slug":"fetaldna-basic-plus","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/en\/fetaldna-basic-plus\/","title":{"rendered":"FETALDNA BASIC PLUS"},"content":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641815715741{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_1641815663675{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”FetalDNA Basic Plus” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

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The FetalDNA Base Plus investigates the 3 main fetal chromosomal aneuploidies related to chromosomes 21, 18,13 and the sex chromosomes X, Y and fetal sex.<\/h3>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row content_placement=”middle” softing_row_prepad=”ptb-30″][vc_column width=”1\/4″][vc_custom_heading text=”Down syndrome” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646089563603{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 2<\/strong>1<\/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][vc_column width=”1\/4″][vc_custom_heading text=”Edwards syndrome” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646089619405{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][vc_column width=”1\/4″][vc_custom_heading text=”Patau syndrome” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646089675048{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][vc_column width=”1\/4″][vc_custom_heading text=”X, Y chromosomes” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1646089717988{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

Sex chromosome aneuploidies<\/strong><\/p>\n

Numerical anomalies of the sex chromosomes.<\/p>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][vc_separator color=”custom” border_width=”2″ accent_color=”#f2483e”][vc_column_text css=”.vc_custom_1671729144827{padding-top: 5% !important;}”]<\/p>\n

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Compared to the FetalDNA Base<\/a>, the FetalDNA Base Plus integrates the aneuplodies of the sex chromosomes<\/em> (anomalies affecting the sex chromosomes X, Y) which can cause language, movement and \/ or learning difficulties in children.<\/p>\n

The most common of this class of aneuploidy is Turner Syndrome<\/em> or X-linked Monosom<\/em>y which affects women with only one copy of the X chromosome.<\/p>\n

Other aneuplodias found with the FetalDNA Base Plus are the Trisomy of the X chromosome (XXX)<\/em>, the Klinefelter Syndrome<\/em> and the Jacobs Syndrome<\/em>.<\/p>\n

Sex of the child available upon request.<\/em><\/p>\n

No information is provided on the other chromosomal abnormalities.<\/em><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/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″ softing_vc_btn_brdclr=”#f2483e” softing_vc_btn_hvrbrdclr=”#f2483e” softing_vc_btn_bg=”#f2483e” softing_vc_btn_hvrbg=”#ffffff” softing_vc_btn_title=”#ffffff” softing_vc_btn_hvrtitle=”#f2483e”][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_message message_box_color=”grey”]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).<\/strong><\/p>\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.<\/strong><\/p>\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.<\/strong>[\/vc_message][\/vc_column][\/vc_row][vc_row full_width=”stretch_row_content” softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”Table comparison” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_single_image source=”external_link” alignment=”center” custom_src=”https:\/\/www.fetaldna.it\/img\/02_ComparativeTable_FetalDNA_BasicPlus_EN.png”][\/vc_column][\/vc_row][vc_row content_placement=”top” softing_row_prepad=”ptb-30″ el_id=”microdeletions”][vc_column][vc_separator color=”custom” border_width=”2″ accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row][vc_column][vc_custom_heading text=”FetalDNA Basic Plus + 90 microdeletions” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

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It is also possible to combine this level with the search for 90 microdeletions, which are anomalies characterized by the absence of a small chromosomal tract with consequent loss of gene information (microdeletions) or by the addition of supernumerary genomic material (microduplications):<\/h3>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_row_inner equal_height=”yes”][vc_column_inner width=”1\/4″][vc_custom_heading text=”DiGeorge syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090454949{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Jacobsen syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090476777{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Langer-Giedion syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090497154{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Wolf-Hirschhorn syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090511281{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_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Kleefstra syndrome (KS)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090534460{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Phelan-Mcdermid syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090551979{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Smith-Magenis syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090568280{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”1q21.1 deletion syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090583756{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_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”WAGR syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090594095{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Potocki-Shaffer syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090604996{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Angelman syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090617270{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Rubinstein-Taybi syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090639780{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_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Koolen-de Vries syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090653085{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”18q deletion syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090664444{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Alagille Syndrome (AGS)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090674707{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”1p36 deletion syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090686827{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_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Williams syndrome” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090702780{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Cri-du-chat syndrome
\n(deletion 5p)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090721310{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Prader-Willi syndrome
\n(15q11-q13)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090742117{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_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Hereditary neuropathy with susceptibility to pressure paralysis (HNPP)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090756833{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_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Miller-Dieker syndrome or lissencephaly type 1 from LIS 1 abnormalities or Miller-Dieker syndrome (MDS)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1646090768294{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_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][vc_column_text css=”.vc_custom_1646090854297{padding-top: 5% !important;}”]<\/p>\n

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Sex of the child available upon request.<\/em><\/p>\n

No information is provided on the other chromosomal abnormalities.<\/em><\/p>\n

In the event that the mother has a negative Rh factor (which can be documented and visible at the time of the FetalDNA request), it is possible to request a free fetal RH analysis.<\/em><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/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 COUNCELLING” style=”effect” size=”lg” softing_vc_btn_brdstyle=”solid” link=”url:tel%3A068505800″ softing_vc_btn_brdclr=”#f2483e” softing_vc_btn_hvrbrdclr=”#f2483e” softing_vc_btn_bg=”#f2483e” softing_vc_btn_hvrbg=”#ffffff” softing_vc_btn_title=”#ffffff” softing_vc_btn_hvrtitle=”#f2483e”][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row][vc_column][vc_message message_box_color=”grey”]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).<\/strong><\/p>\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.<\/strong><\/p>\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.<\/strong>[\/vc_message][\/vc_column][\/vc_row][vc_row full_width=”stretch_row_content” softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”Table comparison” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_single_image source=”external_link” external_img_size=”small” alignment=”center” custom_src=”https:\/\/www.fetaldna.it\/img\/03_ComparativeTable_FetalDNA_BasicPlus90_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_1641815715741{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_1641815663675{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”FetalDNA Basic Plus” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text] The FetalDNA Base Plus investigates the 3 main fetal chromosomal aneuploidies related to chromosomes 21, 18,13 and the sex chromosomes X, Y and fetal sex. 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