{"id":7634,"date":"2022-05-06T02:06:22","date_gmt":"2022-05-06T02:06:22","guid":{"rendered":"https:\/\/www.ggasia.com.my\/?post_type=product&#038;p=7634"},"modified":"2022-05-12T09:14:16","modified_gmt":"2022-05-12T09:14:16","slug":"prenatal-diagnosis-of-fetal-thalassemia","status":"publish","type":"product","link":"https:\/\/www.ggasia.com.my\/cn\/services\/prenatal-diagnosis-of-fetal-thalassemia\/","title":{"rendered":"Prenatal Diagnosis of Fetal Thalassemia"},"content":{"rendered":"<section class=\"vc_row wpb_row vc_row-fluid liquid-row-shadowbox-69e1f4d2e34a8 vc_row-o-equal-height vc_row-o-content-middle vc_row-flex\"><div class=\"ld-container container\"><div class=\"row ld-row\"><div class=\"wpb_column vc_column_container vc_col-sm-1\/5 liquid-column-69e1f4d2e40b0\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><style>.ld_button_69e1f4d2e429d.btn-icon-solid .btn-icon{background:rgb(226, 255, 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127);}.ld_button_69e1f4d2e429d:hover .btn-gradient-border defs stop:last-child{stop-color:rgb(14, 158, 127);}<\/style><a href=\"#first-tab\" class=\"btn btn-solid btn-sm round btn-bordered border-thin ld_button_69e1f4d2e429d\">\n\t<span>\n\t\t\n\t\t\t\t\t<span class=\"btn-txt\">\u6982\u8ff0<\/span>\n\t\t\t\n\t\t\t\t<\/span>\n<\/a>\n<\/div><\/div><\/div><\/div><div class=\"wpb_column vc_column_container vc_col-sm-1\/5 liquid-column-69e1f4d2e51d5\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><style>.ld_button_69e1f4d2e5308.btn-icon-solid .btn-icon{background:rgb(226, 255, 250);}.ld_button_69e1f4d2e5308.btn-icon-circle.btn-icon-ripple .btn-icon:before{border-color:rgb(226, 255, 250);}.ld_button_69e1f4d2e5308.btn-icon-solid:hover .btn-icon{background:rgb(14, 158, 127);}.ld_button_69e1f4d2e5308{background-color:rgb(226, 255, 250);border-color:rgb(226, 255, 250);color:rgb(0, 0, 0);font-weight:600 !important;}.ld_button_69e1f4d2e5308:hover{background-color:rgb(14, 158, 127);border-color:rgb(14, 158, 127);color:rgb(255, 255, 255);}.ld_button_69e1f4d2e5308 .btn-gradient-bg-hover{background:-webkit-linear-gradient(to right, rgb(14, 158, 127) 0%, rgb(14, 158, 127) 100%);background:linear-gradient(to right, rgb(14, 158, 127) 0%, rgb(14, 158, 127) 100%);}.ld_button_69e1f4d2e5308 .btn-gradient-border defs stop:first-child{stop-color:rgb(226, 255, 250);}.ld_button_69e1f4d2e5308 .btn-gradient-border defs stop:last-child{stop-color:rgb(226, 255, 250);}.ld_button_69e1f4d2e5308:hover .btn-gradient-border defs stop:first-child{stop-color:rgb(14, 158, 127);}.ld_button_69e1f4d2e5308:hover .btn-gradient-border defs stop:last-child{stop-color:rgb(14, 158, 127);}<\/style><a href=\"#second-tab\" class=\"btn btn-solid btn-sm round btn-bordered border-thin ld_button_69e1f4d2e5308\">\n\t<span>\n\t\t\n\t\t\t\t\t<span class=\"btn-txt\">\u6587\u4ef6\u8d44\u6599<\/span>\n\t\t\t\n\t\t\t\t<\/span>\n<\/a>\n<\/div><\/div><\/div><\/div><div class=\"wpb_column vc_column_container vc_col-sm-1\/5 liquid-column-69e1f4d2e5cf6\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><\/div><\/div><\/div><\/div><div class=\"wpb_column vc_column_container vc_col-sm-1\/5 liquid-column-69e1f4d2e5f43\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><\/div><\/div><\/div><\/div><div class=\"wpb_column vc_column_container vc_col-sm-1\/5 liquid-column-69e1f4d2e615c\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><\/div><\/div><\/div><\/div><\/div><\/div><\/section><section data-bg-image=\"url\" class=\"vc_row wpb_row vc_row-fluid overview vc_custom_1612338812354 row-contains-padding-top row-contains-padding-bottom liquid-row-shadowbox-69e1f4d2e636e vc_row-has-fill vc_row-has-bg vc_row-o-equal-height vc_row-o-content-middle vc_row-flex\"><div class=\"ld-container container\"><div class=\"row ld-row\"><div class=\"wpb_column vc_column_container vc_col-sm-10 liquid-column-69e1f4d2e6636\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\">\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p>DNA analysis provides definitive diagnosis of thalassemia trait and determines the genotype of the fetal by amniotic fluid. This test is designed to detect deletions in alpha\u0002globin genes (HBA1 and HBA2) and mutations in beta-globin gene (HBB).<\/p>\n\n\t\t<\/div>\n\t<\/div>\n<\/div><\/div><\/div><\/div><div class=\"wpb_column vc_column_container vc_col-sm-2 liquid-column-69e1f4d2e6d4a\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><style>.ld_button_69e1f4d2e6e4a.btn-icon-solid .btn-icon{background:rgb(14, 158, 127);}.ld_button_69e1f4d2e6e4a.btn-icon-circle.btn-icon-ripple .btn-icon:before{border-color:rgb(14, 158, 127);}.ld_button_69e1f4d2e6e4a.btn-icon-solid:hover .btn-icon{background:rgb(226, 255, 250);}.ld_button_69e1f4d2e6e4a{background-color:rgb(14, 158, 127);border-color:rgb(14, 158, 127);color:rgb(255, 255, 255);font-weight:600 !important;}.ld_button_69e1f4d2e6e4a:hover{background-color:rgb(226, 255, 250);border-color:rgb(226, 255, 250);color:rgb(0, 0, 0);}.ld_button_69e1f4d2e6e4a .btn-gradient-bg-hover{background:-webkit-linear-gradient(to right, rgb(226, 255, 250) 0%, rgb(226, 255, 250) 100%);background:linear-gradient(to right, rgb(226, 255, 250) 0%, rgb(226, 255, 250) 100%);}.ld_button_69e1f4d2e6e4a .btn-gradient-border defs stop:first-child{stop-color:rgb(14, 158, 127);}.ld_button_69e1f4d2e6e4a .btn-gradient-border defs stop:last-child{stop-color:rgb(14, 158, 127);}.ld_button_69e1f4d2e6e4a:hover .btn-gradient-border defs stop:first-child{stop-color:rgb(226, 255, 250);}.ld_button_69e1f4d2e6e4a:hover .btn-gradient-border defs stop:last-child{stop-color:rgb(226, 255, 250);}<\/style><a href=\"https:\/\/www.ggasia.com.my\/cn\/#wow-modal-id-1\" class=\"btn btn-solid btn-sm round btn-bordered border-thin ld_button_69e1f4d2e6e4a\">\n\t<span>\n\t\t\n\t\t\t\t\t<span class=\"btn-txt\">\u8054\u7cfb\u6211\u4eec<\/span>\n\t\t\t\n\t\t\t\t<\/span>\n<\/a>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/section><section id=\"first-tab\" class=\"vc_row wpb_row vc_row-fluid liquid-row-shadowbox-69e1f4d2e737e\"><div class=\"ld-container container\"><div class=\"row ld-row\"><div class=\"wpb_column vc_column_container vc_col-sm-12 liquid-column-69e1f4d2e763e\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><h3 style=\"text-align: left\" class=\"vc_custom_heading\"  >\u6982\u8ff0<\/h3><div class=\"vc_tta-container\" data-vc-action=\"collapse\"><div class=\"vc_general vc_tta vc_tta-tabs vc_tta-color-grey vc_tta-style-classic vc_tta-shape-rounded vc_tta-spacing-1 vc_tta-o-no-fill vc_tta-tabs-position-top vc_tta-controls-align-left\"><div class=\"vc_tta-tabs-container\"><ul class=\"vc_tta-tabs-list\"><li class=\"vc_tta-tab vc_active\" data-vc-tab><a href=\"#1611286713015-43107a87-1cdb\" data-vc-tabs data-vc-container=\".vc_tta\"><span class=\"vc_tta-title-text\">Prenatal Diagnosis of Fetal Thalassemia<\/span><\/a><\/li><li class=\"vc_tta-tab\" data-vc-tab><a href=\"#1611286713043-a56b28af-9369\" data-vc-tabs data-vc-container=\".vc_tta\"><span class=\"vc_tta-title-text\">\u7279\u5f81<\/span><\/a><\/li><\/ul><\/div><div class=\"vc_tta-panels-container\"><div class=\"vc_tta-panels\"><div class=\"vc_tta-panel vc_active\" id=\"1611286713015-43107a87-1cdb\" data-vc-content=\".vc_tta-panel-body\"><div class=\"vc_tta-panel-heading\"><h4 class=\"vc_tta-panel-title\"><a href=\"#1611286713015-43107a87-1cdb\" data-vc-accordion data-vc-container=\".vc_tta-container\"><span class=\"vc_tta-title-text\">Prenatal Diagnosis of Fetal Thalassemia<\/span><\/a><\/h4><\/div><div class=\"vc_tta-panel-body\">\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p>Thalassemia is an inherited blood disorder caused by defects in the synthesis of one or more of the hemoglobin chains. There are two main types &#8211; alpha and beta thalassemia. Signs and symptoms vary but may include mild to severe anemia, paleness, fatigue, yellow discoloration of skin (jaundice), and bone problems.<\/p>\n<p>Both thalassemias are inherited in an autosomal recessive manner. Silent carriers of alpha thalassemia and persons with alpha or beta thalassemia trait are asymptomatic and require no treatment.<\/p>\n\n\t\t<\/div>\n\t<\/div>\n<div class=\"vc_empty_space\"   style=\"height: 32px\"><span class=\"vc_empty_space_inner\"><\/span><\/div>\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p><em><img loading=\"lazy\" class=\"wp-image-7635 size-full aligncenter\" src=\"https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia.jpg\" alt=\"\" width=\"543\" height=\"203\" srcset=\"https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia.jpg 543w, https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia-300x112.jpg 300w, https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia-18x7.jpg 18w\" sizes=\"(max-width: 543px) 100vw, 543px\" \/><\/em><\/p>\n\n\t\t<\/div>\n\t<\/div>\n<div class=\"vc_empty_space\"   style=\"height: 32px\"><span class=\"vc_empty_space_inner\"><\/span><\/div>\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p>Alpha (\u03b1) thalassemia is caused by mutations in the HBA1 and\/or HBA2 genes, which leads to reduction or absent synthesis of alpha globin chains. Alpha thalassemia major with hemoglobin Bart&#8217;s usually results in fatal hydrops fetalis. Alpha thalassemia intermedia, or hemoglobin H disease, causes hemolytic anemia.<\/p>\n<p>Beta (\u03b2) thalassemia is caused by mutations in the HBB gene, which leads to reduction or absent synthesis of beta globin chains. Beta thalassemia major causes hemolytic anemia, poor growth, and skeletal abnormalities during infancy. Affected children will require regular lifelong blood transfusions. Beta thalassemia intermedia is less severe than beta thalassemia major and may require episodic blood transfusions.<\/p>\n\n\t\t<\/div>\n\t<\/div>\n<div class=\"vc_empty_space\"   style=\"height: 32px\"><span class=\"vc_empty_space_inner\"><\/span><\/div>\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p><img loading=\"lazy\" class=\"aligncenter wp-image-7636 size-full\" src=\"https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia-2.jpg\" alt=\"\" width=\"1182\" height=\"634\" srcset=\"https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia-2.jpg 1182w, https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia-2-300x161.jpg 300w, https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia-2-1024x549.jpg 1024w, https:\/\/www.ggasia.com.my\/wp-content\/uploads\/2022\/05\/Thalassemia-2-18x10.jpg 18w\" sizes=\"(max-width: 1182px) 100vw, 1182px\" \/><\/p>\n\n\t\t<\/div>\n\t<\/div>\n<div class=\"vc_empty_space\"   style=\"height: 32px\"><span class=\"vc_empty_space_inner\"><\/span><\/div>\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p><strong>Indications for testing:<\/strong><\/p>\n<p>\u2713 Differential diagnosis of microcytic anemia<br \/>\n\u2713 Prenatal diagnosis of thalassemia during pregnancies<\/p>\n\n\t\t<\/div>\n\t<\/div>\n<div class=\"vc_empty_space\"   style=\"height: 32px\"><span class=\"vc_empty_space_inner\"><\/span><\/div>\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p><strong>\u68c0\u4f53\u9700\u6c42:<\/strong><\/p>\n<ul>\n<li>Amniotic fluid 10ml \/ CVS 10mg\/ Cord blood 2ml EDTA<br \/>\n(parents Thalassemia report should be provided)<\/li>\n<\/ul>\n\n\t\t<\/div>\n\t<\/div>\n<\/div><\/div><div class=\"vc_tta-panel\" id=\"1611286713043-a56b28af-9369\" data-vc-content=\".vc_tta-panel-body\"><div class=\"vc_tta-panel-heading\"><h4 class=\"vc_tta-panel-title\"><a href=\"#1611286713043-a56b28af-9369\" data-vc-accordion data-vc-container=\".vc_tta-container\"><span class=\"vc_tta-title-text\">\u7279\u5f81<\/span><\/a><\/h4><\/div><div class=\"vc_tta-panel-body\">\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p>Testing Scope :<br \/>\n\u2013 \u03b1-thalassemia (\u03b1\u03b1\/&#8211;) of SEA, Philippine and Thailand type<br \/>\n\u2013 \u03b1-thalassemia (\u03b1\u03b1\/-\u03b1) ) \u03b13.7,\u03b14.2 deletion and HbCS (c.427T&gt;C) ,HbQS(c.377T&gt;C)<br \/>\n\u2013 20 most common \u03b2-thalassemia mutations<\/p>\n\n\t\t<\/div>\n\t<\/div>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section><section id=\"second-tab\" class=\"vc_row wpb_row vc_row-fluid liquid-row-shadowbox-69e1f4d2eb3cb\"><div class=\"ld-container container\"><div class=\"row ld-row\"><div class=\"wpb_column vc_column_container vc_col-sm-12 liquid-column-69e1f4d2eb646\"><div class=\"vc_column-inner\"><div class=\"wpb_wrapper\"   ><div class=\"wpb_wrapper-inner\"><h3 style=\"text-align: left\" class=\"vc_custom_heading\"  >\u6587\u4ef6\u8d44\u6599<\/h3>\n\t<div class=\"wpb_text_column wpb_content_element\" >\n\t\t<div class=\"wpb_wrapper\">\n\t\t\t<p><strong>Brochure<\/strong><\/p>\n\n\t\t<\/div>\n\t<\/div>\n<div class=\"vc_empty_space\"   style=\"height: 20px\"><span class=\"vc_empty_space_inner\"><\/span><\/div><style>.ld_button_69e1f4d2ebc95.btn-icon-solid .btn-icon{background:rgb(14, 158, 127);}.ld_button_69e1f4d2ebc95.btn-icon-circle.btn-icon-ripple .btn-icon:before{border-color:rgb(14, 158, 127);}.ld_button_69e1f4d2ebc95.btn-icon-solid:hover .btn-icon{background:rgb(226, 255, 250);}.ld_button_69e1f4d2ebc95{background-color:rgb(14, 158, 127);border-color:rgb(14, 158, 127);color:rgb(255, 255, 255);font-weight:600 !important;}.ld_button_69e1f4d2ebc95:hover{background-color:rgb(226, 255, 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PDF<\/span>\n\t\t\t\n\t\t\t\t<\/span>\n<\/a>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/section>","protected":false},"excerpt":{"rendered":"Overview Documentation DNA analysis provides definitive diagnosis of thalassemia trait and determines the genotype of...","protected":false},"featured_media":5888,"template":"","meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v16.3 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Prenatal Diagnosis of Fetal Thalassemia - GGA Malaysia<\/title>\n<meta name=\"description\" content=\"SNP microarray is a genetic testing for miscarriage to detect chromosomal abnormalities in POC (products of conception).\" \/>\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.ggasia.com.my\/cn\/services\/prenatal-diagnosis-of-fetal-thalassemia\/\" \/>\n<meta property=\"og:locale\" content=\"zh_TW\" \/>\n<meta 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