{"id":10077,"date":"2025-07-13T21:48:13","date_gmt":"2025-07-13T18:48:13","guid":{"rendered":"https:\/\/medilab.km.ua\/?p=10077"},"modified":"2026-04-20T18:53:39","modified_gmt":"2026-04-20T15:53:39","slug":"diagnosis-of-chromosomal-disorders-current-approaches-and-possibilities","status":"publish","type":"post","link":"https:\/\/medilab.km.ua\/en\/diagnosis-of-chromosomal-disorders-current-approaches-and-possibilities\/","title":{"rendered":"Diagnosis of chromosomal disorders: modern approaches and possibilities"},"content":{"rendered":"<div class=\"kk-star-ratings kksr-auto kksr-align-left kksr-valign-top\"\n    data-payload='{&quot;align&quot;:&quot;left&quot;,&quot;id&quot;:&quot;10077&quot;,&quot;slug&quot;:&quot;default&quot;,&quot;valign&quot;:&quot;top&quot;,&quot;ignore&quot;:&quot;&quot;,&quot;reference&quot;:&quot;auto&quot;,&quot;class&quot;:&quot;&quot;,&quot;count&quot;:&quot;722&quot;,&quot;legendonly&quot;:&quot;&quot;,&quot;readonly&quot;:&quot;&quot;,&quot;score&quot;:&quot;4.9&quot;,&quot;starsonly&quot;:&quot;&quot;,&quot;best&quot;:&quot;5&quot;,&quot;gap&quot;:&quot;5&quot;,&quot;greet&quot;:&quot;Rate this post&quot;,&quot;legend&quot;:&quot;4.9\\\/5 - (722 votes)&quot;,&quot;size&quot;:&quot;24&quot;,&quot;title&quot;:&quot;\u0414\u0456\u0430\u0433\u043d\u043e\u0441\u0442\u0438\u043a\u0430 \u0445\u0440\u043e\u043c\u043e\u0441\u043e\u043c\u043d\u0438\u0445 \u043f\u043e\u0440\u0443\u0448\u0435\u043d\u044c: \u0441\u0443\u0447\u0430\u0441\u043d\u0456 \u043f\u0456\u0434\u0445\u043e\u0434\u0438 \u0442\u0430 \u043c\u043e\u0436\u043b\u0438\u0432\u043e\u0441\u0442\u0456&quot;,&quot;width&quot;:&quot;139.6&quot;,&quot;_legend&quot;:&quot;{score}\\\/{best} - ({count} {votes})&quot;,&quot;font_factor&quot;:&quot;1.25&quot;}'>\n            \n<div class=\"kksr-stars\">\n    \n<div class=\"kksr-stars-inactive\">\n            <div class=\"kksr-star\" data-star=\"1\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"2\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"3\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"4\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"5\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n    <\/div>\n    \n<div class=\"kksr-stars-active\" style=\"width: 139.6px;\">\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n    <\/div>\n<\/div>\n                \n\n<div class=\"kksr-legend\" style=\"font-size: 19.2px;\">\n            4.9\/5 - (722 votes)    <\/div>\n    <\/div>\n<p data-start=\"253\" data-end=\"762\">\n<p data-start=\"253\" data-end=\"762\">\n<p data-start=\"253\" data-end=\"762\">\n<p data-start=\"253\" data-end=\"762\">Chromosomes are structured complexes of DNA that contain genetic information about our body. Normally, each person has 46 chromosomes (23 pairs), but sometimes malfunctions occur that lead to changes in the number or structure of these carriers of the genetic code. Such changes can cause serious diseases, affect the development of the child, or cause reproductive problems. Timely <strong data-start=\"629\" data-end=\"665\">diagnosis of chromosomal disorders<\/strong> helps not only to identify pathologies, but also to correctly assess the risks for the future generation.<\/p>\n<h2 data-start=\"764\" data-end=\"803\">Why do chromosomal abnormalities occur?<\/h2>\n<p data-start=\"805\" data-end=\"842\">The main reasons for such changes include:<\/p>\n<ul data-start=\"843\" data-end=\"1118\">\n<li data-start=\"843\" data-end=\"889\">\n<p data-start=\"845\" data-end=\"889\"><strong data-start=\"845\" data-end=\"866\">Spontaneous mutations<\/strong> during cell division;<\/p>\n<\/li>\n<li data-start=\"890\" data-end=\"941\">\n<p data-start=\"892\" data-end=\"941\"><strong data-start=\"892\" data-end=\"907\">Age of parents<\/strong>, especially mothers over 35 years of age;<\/p>\n<\/li>\n<li data-start=\"942\" data-end=\"993\">\n<p data-start=\"944\" data-end=\"993\"><strong data-start=\"944\" data-end=\"992\">Exposure to toxins, radiation, and chemicals<\/strong>;<\/p>\n<\/li>\n<li data-start=\"994\" data-end=\"1048\">\n<p data-start=\"996\" data-end=\"1048\"><strong data-start=\"996\" data-end=\"1029\">Disorders during fertilization<\/strong> (meiosis abnormalities);<\/p>\n<\/li>\n<li data-start=\"1049\" data-end=\"1118\">\n<p data-start=\"1051\" data-end=\"1118\"><strong data-start=\"1051\" data-end=\"1089\">Hereditary translocations or inversions<\/strong>, that are passed down from parents.<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"1120\" data-end=\"1248\">It is important to remember that chromosomal abnormalities can be not only hereditary, but also occur for the first time in a particular embryo or child.<\/p>\n<h2 data-start=\"1255\" data-end=\"1290\">When should chromosomes be checked?<\/h2>\n<p data-start=\"1292\" data-end=\"1367\">There are several key situations where diagnostics are necessary or highly desirable:<\/p>\n<ul data-start=\"1368\" data-end=\"1781\">\n<li data-start=\"1368\" data-end=\"1477\">\n<p data-start=\"1370\" data-end=\"1477\"><strong data-start=\"1370\" data-end=\"1403\">When planning a pregnancy<\/strong>, especially if there is a family history of miscarriages or problems conceiving.<\/p>\n<\/li>\n<li data-start=\"1478\" data-end=\"1564\">\n<p data-start=\"1480\" data-end=\"1564\"><strong data-start=\"1480\" data-end=\"1514\">If a child has developmental delay<\/strong>, the presence of congenital defects or unexplained conditions.<\/p>\n<\/li>\n<li data-start=\"1565\" data-end=\"1614\">\n<p data-start=\"1567\" data-end=\"1614\"><strong data-start=\"1567\" data-end=\"1613\">In case of infertility or unsuccessful IVF attempts<\/strong>.<\/p>\n<\/li>\n<li data-start=\"1615\" data-end=\"1707\">\n<p data-start=\"1617\" data-end=\"1707\"><strong data-start=\"1617\" data-end=\"1660\">For suspected known genetic syndromes<\/strong>: Down, Edwards, Turner, Klinefelter, etc.<\/p>\n<\/li>\n<li data-start=\"1708\" data-end=\"1781\">\n<p data-start=\"1710\" data-end=\"1781\"><strong data-start=\"1710\" data-end=\"1749\">As part of prenatal diagnosis<\/strong> \u2014 to check the health of the fetus.<\/p>\n<\/li>\n<\/ul>\n<h2 data-start=\"1788\" data-end=\"1824\">The most common chromosomal syndromes<\/h2>\n<ol data-start=\"1826\" data-end=\"2324\">\n<li data-start=\"1826\" data-end=\"1943\">\n<p data-start=\"1829\" data-end=\"1943\"><strong data-start=\"1829\" data-end=\"1872\">Down syndrome (<a href=\"https:\/\/medilab.km.ua\/en\/price\/?3325_search_1=%D1%82%D1%80%D0%B8%D1%81%D0%BE%D0%BC%D1%96%D1%8F%2021-%D1%97%20%D1%85%D1%80%D0%BE%D0%BC%D0%BE%D1%81%D0%BE%D0%BC%D0%B8&amp;3325_device=laptop&amp;3325_orderby=relevance&amp;3325_paged=1&amp;3325_filtered=true\">trisomy of the 21st chromosome<\/a>)<\/strong> \u2014 causes mental retardation and characteristic external features.<\/p>\n<\/li>\n<li data-start=\"1944\" data-end=\"2040\">\n<p data-start=\"1947\" data-end=\"2040\"><strong data-start=\"1947\" data-end=\"1993\">Edwards syndrome (trisomy 18)<\/strong> \u2014 accompanied by serious organ defects.<\/p>\n<\/li>\n<li data-start=\"2041\" data-end=\"2138\">\n<p data-start=\"2044\" data-end=\"2138\"><strong data-start=\"2044\" data-end=\"2087\">Patau syndrome (trisomy of chromosome 13)<\/strong> \u2014 severe defects of the nervous system, heart, and face.<\/p>\n<\/li>\n<li data-start=\"2139\" data-end=\"2243\">\n<p data-start=\"2142\" data-end=\"2243\"><strong data-start=\"2142\" data-end=\"2184\">Turner syndrome (monosomy X in girls)<\/strong> \u2014 causes problems with growth, development, and fertility.<\/p>\n<\/li>\n<li data-start=\"2244\" data-end=\"2324\">\n<p data-start=\"2247\" data-end=\"2324\"><strong data-start=\"2247\" data-end=\"2288\">Klinefelter syndrome (XXY in boys)<\/strong> \u2014 hormonal disorders, infertility.<\/p>\n<\/li>\n<\/ol>\n<p data-start=\"2326\" data-end=\"2410\">Diagnostics helps to detect these conditions early in pregnancy or even before conception.<\/p>\n<h2 data-start=\"2417\" data-end=\"2459\">Methods for diagnosing chromosomal disorders<\/h2>\n<div class=\"_tableContainer_80l1q_1\">\n<div class=\"_tableWrapper_80l1q_14 group flex w-fit flex-col-reverse\">\n<table class=\"w-fit min-w-(--thread-content-width)\" data-start=\"2461\" data-end=\"3188\">\n<thead data-start=\"2461\" data-end=\"2517\">\n<tr data-start=\"2461\" data-end=\"2517\">\n<th data-start=\"2461\" data-end=\"2469\" data-col-size=\"sm\">Method<\/th>\n<th data-start=\"2469\" data-end=\"2486\" data-col-size=\"md\">Working principle<\/th>\n<th data-start=\"2486\" data-end=\"2500\" data-col-size=\"md\">What determines<\/th>\n<th data-start=\"2500\" data-end=\"2517\" data-col-size=\"sm\">Execution time<\/th>\n<\/tr>\n<\/thead>\n<tbody data-start=\"2576\" data-end=\"3188\">\n<tr data-start=\"2576\" data-end=\"2707\">\n<td data-start=\"2576\" data-end=\"2597\" data-col-size=\"sm\"><strong data-start=\"2578\" data-end=\"2596\">Karyotyping<\/strong><\/td>\n<td data-start=\"2597\" data-end=\"2645\" data-col-size=\"md\">Microscopic analysis of chromosomes from blood cells<\/td>\n<td data-start=\"2645\" data-end=\"2694\" data-col-size=\"md\">Major changes: trisomies, translocations, inversions<\/td>\n<td data-start=\"2694\" data-end=\"2707\" data-col-size=\"sm\">2\u20133 weeks<\/td>\n<\/tr>\n<tr data-start=\"2708\" data-end=\"2820\">\n<td data-start=\"2708\" data-end=\"2719\" data-col-size=\"sm\"><strong data-start=\"2710\" data-end=\"2718\">FISH<\/strong><\/td>\n<td data-start=\"2719\" data-end=\"2775\" data-col-size=\"md\">Fluorescent probes for labeling specific DNA regions<\/td>\n<td data-start=\"2775\" data-end=\"2808\" data-col-size=\"md\">Microdeletions, point anomalies<\/td>\n<td data-start=\"2808\" data-end=\"2820\" data-col-size=\"sm\">2\u20135 days<\/td>\n<\/tr>\n<tr data-start=\"2821\" data-end=\"2929\">\n<td data-start=\"2821\" data-end=\"2834\" data-col-size=\"sm\"><strong data-start=\"2823\" data-end=\"2833\">QF-PCR<\/strong><\/td>\n<td data-start=\"2834\" data-end=\"2890\" data-col-size=\"md\">Rapid gene copy number analysis using PCR<\/td>\n<td data-start=\"2890\" data-end=\"2918\" data-col-size=\"md\">Trisomies 13, 18, 21, X, Y<\/td>\n<td data-start=\"2918\" data-end=\"2929\" data-col-size=\"sm\">1\u20132 days<\/td>\n<\/tr>\n<tr data-start=\"2930\" data-end=\"3056\">\n<td data-start=\"2930\" data-end=\"2975\" data-col-size=\"sm\"><strong data-start=\"2932\" data-end=\"2974\">CGH (comparative genomic hybridization)<\/strong><\/td>\n<td data-start=\"2975\" data-end=\"3012\" data-col-size=\"md\">Comparison of patient DNA with a reference<\/td>\n<td data-start=\"3012\" data-end=\"3043\" data-col-size=\"md\">Small duplications and deletions<\/td>\n<td data-start=\"3043\" data-end=\"3056\" data-col-size=\"sm\">1\u20132 weeks<\/td>\n<\/tr>\n<tr data-start=\"3057\" data-end=\"3188\">\n<td data-start=\"3057\" data-end=\"3099\" data-col-size=\"sm\"><strong data-start=\"3059\" data-end=\"3098\">NGS (<a href=\"https:\/\/medilab.km.ua\/en\/sequencing-of-the-new-generation-of-ngs-answers-to-the-main-question\/\">next generation sequencing<\/a>)<\/strong><\/td>\n<td data-start=\"3099\" data-end=\"3133\" data-col-size=\"md\">Analysis of millions of DNA fragments<\/td>\n<td data-start=\"3133\" data-end=\"3175\" data-col-size=\"md\">All types of changes \u2014 from major to minor<\/td>\n<td data-start=\"3175\" data-end=\"3188\" data-col-size=\"sm\">1\u20133 weeks<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<div class=\"sticky end-(--thread-content-margin) h-0 self-end select-none\">\n<div class=\"absolute end-0 flex items-end\"><\/div>\n<\/div>\n<\/div>\n<\/div>\n<h2 data-start=\"3195\" data-end=\"3228\">Prenatal diagnostic methods<\/h2>\n<p data-start=\"3230\" data-end=\"3255\"><strong data-start=\"3230\" data-end=\"3252\">Non-invasive methods<\/strong>:<\/p>\n<ul data-start=\"3256\" data-end=\"3496\">\n<li data-start=\"3256\" data-end=\"3405\">\n<p data-start=\"3258\" data-end=\"3405\"><strong data-start=\"3258\" data-end=\"3299\">NIPT (non-invasive prenatal test)<\/strong> \u2014 fetal DNA analysis in the mother&#039;s blood. The safest and provides accuracy of over 99% for the most common anomalies.<\/p>\n<\/li>\n<li data-start=\"3406\" data-end=\"3496\">\n<p data-start=\"3408\" data-end=\"3496\"><strong data-start=\"3408\" data-end=\"3444\">First and second trimester ultrasound<\/strong> \u2014 detects anatomical markers of chromosomal syndromes.<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"3498\" data-end=\"3521\"><strong data-start=\"3498\" data-end=\"3518\">Invasive methods<\/strong>:<\/p>\n<ul data-start=\"3522\" data-end=\"3758\">\n<li data-start=\"3522\" data-end=\"3606\">\n<p data-start=\"3524\" data-end=\"3606\"><strong data-start=\"3524\" data-end=\"3539\">Amniocentesis<\/strong> \u2014 amniotic fluid sampling for genetic analysis (from week 15).<\/p>\n<\/li>\n<li data-start=\"3607\" data-end=\"3691\">\n<p data-start=\"3609\" data-end=\"3691\"><strong data-start=\"3609\" data-end=\"3628\">Chorionic biopsy<\/strong> \u2014 analysis of placental cells in the early stages (from 10\u201311 weeks).<\/p>\n<\/li>\n<li data-start=\"3692\" data-end=\"3758\">\n<p data-start=\"3694\" data-end=\"3758\"><strong data-start=\"3694\" data-end=\"3709\">Cordocentesis<\/strong> \u2014 umbilical cord blood test (after 18 weeks).<\/p>\n<\/li>\n<\/ul>\n<h2 data-start=\"3765\" data-end=\"3792\"><img decoding=\"async\" class=\"alignnone size-full wp-image-10080\" src=\"https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/07\/ginekolog-provodit-ul-trazvukovuu-konsul-taciu.jpg\" alt=\"a geneticist advises a couple before pregnancy\" width=\"1200\" height=\"800\" srcset=\"https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/07\/ginekolog-provodit-ul-trazvukovuu-konsul-taciu.jpg 1200w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/07\/ginekolog-provodit-ul-trazvukovuu-konsul-taciu-150x100.jpg 150w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/07\/ginekolog-provodit-ul-trazvukovuu-konsul-taciu-600x400.jpg 600w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/07\/ginekolog-provodit-ul-trazvukovuu-konsul-taciu-300x200.jpg 300w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/07\/ginekolog-provodit-ul-trazvukovuu-konsul-taciu-1024x683.jpg 1024w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/07\/ginekolog-provodit-ul-trazvukovuu-konsul-taciu-768x512.jpg 768w\" sizes=\"(max-width: 1200px) 100vw, 1200px\" \/><\/h2>\n<h2 data-start=\"3765\" data-end=\"3792\">Genetic counseling<\/h2>\n<p data-start=\"3794\" data-end=\"3854\">After receiving the analysis results, the geneticist helps:<\/p>\n<ul data-start=\"3855\" data-end=\"4006\">\n<li data-start=\"3855\" data-end=\"3890\">\n<p data-start=\"3857\" data-end=\"3890\">explain the significance of the identified changes;<\/p>\n<\/li>\n<li data-start=\"3891\" data-end=\"3934\">\n<p data-start=\"3893\" data-end=\"3934\">assess risks for future pregnancies;<\/p>\n<\/li>\n<li data-start=\"3935\" data-end=\"4006\">\n<p data-start=\"3937\" data-end=\"4006\">to offer individual tactics for pregnancy management or treatment.<\/p>\n<\/li>\n<\/ul>\n<h2 data-start=\"4013\" data-end=\"4033\">Modern innovations<\/h2>\n<ul data-start=\"4035\" data-end=\"4384\">\n<li data-start=\"4035\" data-end=\"4168\">\n<p data-start=\"4037\" data-end=\"4168\"><a href=\"https:\/\/medilab.km.ua\/en\/artificial-intelligence-in-medicine-as-a-technology-that-changes-the-health-care-system\/\"><strong data-start=\"4037\" data-end=\"4057\">Artificial intelligence<\/strong><\/a> is used for automatic analysis of karyotypes and FISH images, which significantly reduces diagnostic time.<\/p>\n<\/li>\n<li data-start=\"4169\" data-end=\"4265\">\n<p data-start=\"4171\" data-end=\"4265\"><strong data-start=\"4171\" data-end=\"4197\">Microchip technologies<\/strong> allow scanning tens of thousands of genetic markers simultaneously.<\/p>\n<\/li>\n<li data-start=\"4266\" data-end=\"4384\">\n<p data-start=\"4268\" data-end=\"4384\"><strong data-start=\"4268\" data-end=\"4298\">Next-generation NGS tests<\/strong> capable of detecting even minimal DNA rearrangements that previously went unnoticed.<\/p>\n<\/li>\n<\/ul>\n<h2 data-start=\"4391\" data-end=\"4415\">Frequently Asked Questions (FAQ)<\/h2>\n<p data-start=\"4417\" data-end=\"4591\"><strong data-start=\"4417\" data-end=\"4492\">1. Can all chromosomal diseases be detected with one test?<\/strong><br data-start=\"4492\" data-end=\"4495\" \/>No, each method has its limitations. The most complete analysis is provided by NGS or karyotyping combined with FISH.<\/p>\n<p data-start=\"4593\" data-end=\"4765\"><strong data-start=\"4593\" data-end=\"4639\">2. Are invasive methods safe for the fetus?<\/strong><br data-start=\"4639\" data-end=\"4642\" \/>Amniocentesis or chorionic villus sampling has a small risk (about 0.1\u20130.31% of the time), so it is only performed when medically indicated.<\/p>\n<p data-start=\"4767\" data-end=\"4889\"><strong data-start=\"4767\" data-end=\"4815\">3. Is preparation required for karyotyping?<\/strong><br data-start=\"4815\" data-end=\"4818\" \/>There is no special preparation. The study is performed on venous blood.<\/p>\n<p data-start=\"4891\" data-end=\"5001\"><strong data-start=\"4891\" data-end=\"4946\">4. Can I have a chromosome analysis after giving birth?<\/strong><br data-start=\"4946\" data-end=\"4949\" \/>Yes, karyotyping can be done at any age.<\/p>\n<h2 data-start=\"5008\" data-end=\"5041\">The importance of early diagnosis<\/h2>\n<p data-start=\"5043\" data-end=\"5085\">Diagnosis of chromosomal disorders allows:<\/p>\n<ul data-start=\"5086\" data-end=\"5282\">\n<li data-start=\"5086\" data-end=\"5133\">\n<p data-start=\"5088\" data-end=\"5133\">timely identify risks in the unborn child;<\/p>\n<\/li>\n<li data-start=\"5134\" data-end=\"5182\">\n<p data-start=\"5136\" data-end=\"5182\">prevent the birth of a child with severe disabilities;<\/p>\n<\/li>\n<li data-start=\"5183\" data-end=\"5232\">\n<p data-start=\"5185\" data-end=\"5232\">choose the right tactics for managing pregnancy;<\/p>\n<\/li>\n<li data-start=\"5233\" data-end=\"5282\">\n<p data-start=\"5235\" data-end=\"5282\">obtain valuable information for family planning.<\/p>\n<\/li>\n<\/ul>\n<p>Diagnosis of chromosomal disorders is not only a way to detect problems, but also a way to prevent them, make informed choices, and get accurate information about the health of the unborn child. Early diagnosis reduces risks and gives families a chance to prepare for challenges.<\/p>","protected":false},"excerpt":{"rendered":"<p>Chromosomes are structured complexes of DNA that contain genetic information about our body. Normally, each person has 46 chromosomes.<\/p>","protected":false},"author":627,"featured_media":10079,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-10077","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>\u0414\u0456\u0430\u0433\u043d\u043e\u0441\u0442\u0438\u043a\u0430 \u0445\u0440\u043e\u043c\u043e\u0441\u043e\u043c\u043d\u0438\u0445 \u043f\u043e\u0440\u0443\u0448\u0435\u043d\u044c: \u043c\u0435\u0442\u043e\u0434\u0438, \u0430\u043d\u0430\u043b\u0456\u0437\u0438 \u0442\u0430 \u0442\u0435\u0441\u0442\u0438<\/title>\n<meta name=\"description\" content=\"\u041a\u0430\u0440\u0456\u043e\u0442\u0438\u043f\u0443\u0432\u0430\u043d\u043d\u044f, FISH, NGS, NIPT \u0442\u0430 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Specialist in clinical laboratory diagnostics, clinical biochemistry and immunology. Has over 45 years of practical experience in medicine and laboratory diagnostics. Since 2007, he has been the founder and head of Medi Lab Plus LLC. She began her professional career as a nurse, later worked as an assistant epidemiologist and laboratory assistant. In 1987\u20132007, she headed a centralized serological laboratory. Education and specializations \u2022 1979 \u2014 Khmelnytskyi Basic Medical School, paramedic \u2022 1986 \u2014 Odessa State University named after I.I. Mechnikov, biologist \u2022 2001 \u2014 clinical laboratory diagnostics, NMAPE named after P.L. Shupyk \u2022 2008 \u2014 PCR diagnostics of infectious diseases, Institute of Epidemiology named after L.V. Gromashevsky \u2022 2010, 2015, 2021 \u2014 organization and management of healthcare \u2022 2017 \u2014 clinical laboratory diagnostics, Ukrainian Military Medical Academy \u2022 2017 \u2014 clinical biochemistry, Ukrainian Military Medical Academy \u2022 2018 \u2014 clinical immunology, Ukrainian Military Medical Academy \u2022 2025 \u2014 topical issues of modern medicine and pharmacy, Kharkiv Polytechnic Institute Work experience \u2022 1979\u20131982 \u2014 hospital nurse \u2022 1982\u20131986 \u2014 assistant epidemiologist \u2022 1986\u20131987 \u2014 laboratory assistant \u2022 1987\u20132007 \u2014 head of a centralized serological laboratory \u2022 Since 2007 \u2014 director of Medi Lab Plus LLC Key competencies Organization and management of medical laboratories, implementation of modern methods of laboratory diagnostics (PCR, immunological and biochemical studies), quality control of laboratory processes in accordance with state and international standards.","url":"https:\/\/medilab.km.ua\/en\/author\/medilab-an\/"}]}},"_links":{"self":[{"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/posts\/10077","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/users\/627"}],"replies":[{"embeddable":true,"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/comments?post=10077"}],"version-history":[{"count":0,"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/posts\/10077\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/media\/10079"}],"wp:attachment":[{"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/media?parent=10077"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/categories?post=10077"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/medilab.km.ua\/en\/wp-json\/wp\/v2\/tags?post=10077"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}