58 lines
3.5 KiB
JavaScript
58 lines
3.5 KiB
JavaScript
export default function HereditaryCancerPanel() {
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const features = [
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{ title: "Comprehensive Gene Coverage", desc: "Includes high- and moderate-risk genes such as BRCA1, BRCA2, TP53, MLH1, MSH2, APC, and others." },
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{ title: "Germline Variant Detection", desc: "Accurately detects SNVs, Indels, and selected CNVs in genes associated with inherited cancer risk." },
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{ title: "Family-Centered Testing", desc: "Supports cascade testing for at-risk relatives, enabling early detection and prevention." },
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{ title: "Clinical Actionability", desc: "Provides insights that guide surveillance, preventive measures, and personalized treatment planning." },
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{ title: "High Sensitivity & Specificity", desc: "Uses ≥100X sequencing depth with ≥90% Q30 base quality for reliable variant calling." },
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{ title: "Expert Interpretation & Reporting", desc: "Variants classified using ACMG guidelines, backed by curated literature and clinical databases." },
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{ title: "Genetic Counseling Support", desc: "Optional access to pre- and post-test counseling for patient education and informed decision-making." }
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];
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return (
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<section className="mx-auto px-10 pt-12">
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<h2 className="text-3xl font-bold text-gray-700 text-left pb-2 mb-4">Operify Hereditary Cancer Panel</h2>
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<div className="mb-8">
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<p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
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<strong>About 5-10% of all cancers are linked to inherited genetic mutations</strong>, often going
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undetected until late stages or after multiple family members are affected.
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</p>
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<p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
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The Operify Hereditary Cancer Panel screens key high- and moderate-risk genes associated
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with hereditary cancer syndromes like HBOC, Lynch Syndrome (LS), Li Fraumeni Syndrome (LFS),
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Familial Adenomatous Polyposis (FAP), Cowden Syndrome (CS), Peutz-Jeghers Syndrome (PJS),
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Neurofibromatosis (NF) etc.
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</p>
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<p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
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Early identification of germline mutations enables proactive clinical decisions, including
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risk-reducing strategies, targeted surveillance, and family cascade testing.
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</p>
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<p className="text-gray-600 leading-relaxed text-base text-justify">
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Studies show that genetic testing in hereditary cancer cases improves outcomes and informs
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care for both patients and at-risk relatives.
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</p>
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</div>
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<h3 className="text-2xl font-semibold text-gray-700 mb-4">Key Features</h3>
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<div className="overflow-x-auto">
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<table className="w-full border-collapse border border-gray-300 rounded-lg">
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<thead>
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<tr className="bg-teal-50">
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<th className="border border-gray-300 px-3 py-2 text-left font-semibold text-teal-700">Feature</th>
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<th className="border border-gray-300 px-3 py-2 text-left font-semibold text-teal-700">Description</th>
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</tr>
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</thead>
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<tbody>
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{features.map((feature, idx) => (
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<tr key={idx} className="hover:bg-gray-50">
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<td className="border border-gray-300 px-6 py-3 text-gray-700 font-medium">{feature.title}</td>
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<td className="border border-gray-300 px-6 py-3 text-gray-600">{feature.desc}</td>
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</tr>
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))}
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</tbody>
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</table>
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</div>
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</section>
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);
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} |