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THE ROLE OF GENETIC TESTING IN CLINICAL LABORATORY DIAGNOSTICS OF HEREDITARY DISEASES IN CHILDREN

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dc.contributor.authorGaffarova Sabina Xayrullo qizi
dc.contributor.authorIsomadinova Lola Kamolidinovna
dc.contributor.authorKarimova Linara Alixanovna
dc.date.accessioned2025-12-29T17:57:14Z
dc.date.issued2025-01-25
dc.description.abstractHereditary diseases pose a significant challenge in pediatric medicine due to their diverse manifestations and potential lifelong consequences. Genetic testing has become an essential tool in clinical laboratory diagnostics, offering insights into the underlying genetic causes of these conditions. This article discusses the principles of genetic testing, its applications in diagnosing hereditary diseases in children, and the challenges and prospects of implementing these technologies in clinical practice.
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dc.identifier.urihttps://webofjournals.com/index.php/5/article/view/3023
dc.identifier.urihttps://asianeducationindex.com/handle/123456789/24320
dc.language.isoeng
dc.publisherWeb of Journals Publishing
dc.relationhttps://webofjournals.com/index.php/5/article/view/3023/2987
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourceWeb of Medicine: Journal of Medicine, Practice and Nursing ; Vol. 3 No. 1 (2025): WOM; 237-240
dc.source2938-3765
dc.subjectGenetic testing, hereditary diseases, pediatric diagnostics, next-generation sequencing (NGS), polymerase chain reaction (PCR), congenital disorders, metabolic disorders, chromosomal abnormalities, precision medicine, newborn screening, primary immunodeficiency, cancer predisposition syndromes, gene therapy, personalized medicine, ethical challenges.
dc.titleTHE ROLE OF GENETIC TESTING IN CLINICAL LABORATORY DIAGNOSTICS OF HEREDITARY DISEASES IN CHILDREN
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article

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