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Molecular Pathology Diagnostic Services offer advanced diagnostic testing and analysis to identify and understand diseases at the molecular level. Utilizing cutting-edge technology and sophisticated techniques, our services provide critical insights into genetic, biochemical, and cellular abnormalities that underpin a wide range of health conditions. Our dedicated team of molecular pathologists and laboratory professionals is committed to delivering precise, reliable results that support accurate diagnosis, personalized treatment, and improved patient outcomes. Comprehensive Molecular Pathology Care Our Molecular Pathology Diagnostic Services encompass a variety of specialized tests and analyses designed to detect and characterize diseases at a molecular level: Advanced Molecular Testing: Employing state-of-the-art technology to analyze genetic and molecular markers, including: Genetic Sequencing: High-throughput sequencing techniques, such as next-generation sequencing (NGS), to identify genetic mutations, variations, and inherited disorders that may impact patient health. Polymerase Chain Reaction (PCR): A powerful technique for amplifying and analyzing specific DNA or RNA sequences, used to detect genetic mutations, infectious agents, and gene expression profiles. In Situ Hybridization: Techniques such as fluorescent in situ hybridization (FISH) to visualize and map genetic material within cells, helping to identify chromosomal abnormalities and gene rearrangements. Cancer Genomics: Specialized testing to characterize cancer at a molecular level, including: Tumor Profiling: Analysis of cancerous tissues to identify genetic mutations, gene expression patterns, and biomarkers that inform treatment decisions and prognosis. Minimal Residual Disease (MRD) Detection: Sensitive testing to detect residual cancer cells after treatment, providing insights into disease remission and recurrence risk. Inherited Genetic Disorders: Comprehensive evaluation for genetic conditions, including: Genetic Screening: Testing for hereditary disorders such as cystic fibrosis, muscular dystrophy, and other genetic conditions to provide early diagnosis and family planning information. Carrier Testing: Identifying individuals who carry genetic mutations associated with inherited diseases, helping to assess risk and guide reproductive decisions. Infectious Disease Testing: Advanced diagnostics to identify and characterize pathogens, including: Pathogen Detection: Molecular assays to detect bacteria, viruses, fungi, and parasites, providing accurate and timely diagnosis of infectious diseases. Antimicrobial Resistance Testing: Analyzing genetic markers to determine resistance profiles of pathogens, guiding effective treatment strategies. Patient Education and Support: Providing detailed information and support to help patients understand their test results and implications, including: Results Interpretation: Clear explanations of molecular pathology findings, their significance, and potential impact on treatment and prognosis. Genetic Counseling: Expert guidance on managing genetic risks, interpreting results, and making informed decisions about health and family planning. Collaboration and Coordination: Working closely with healthcare providers to ensure comprehensive care, including: Referral Services: Facilitating access to specialists and additional testing as needed. Follow-Up and Monitoring: Providing ongoing support to track disease progression, treatment response, and long-term outcomes.