99 lines
4.4 KiB
JavaScript
99 lines
4.4 KiB
JavaScript
import React from 'react';
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import Image from 'next/image';
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const FeatureCard = ({ icon, title, description }) => (
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<div className="p-6 rounded-2xl shadow-sm border-0 h-full transition-transform duration-300 ease-in-out hover:scale-105 hover:shadow-lg group" style={{ backgroundColor: '#f2fcfc' }}>
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<div className="flex items-center space-x-4 mb-4">
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<div className="w-12 h-12 bg-orange-100 rounded-xl flex items-center justify-center flex-shrink-0">
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<Image src={icon} alt={title} width={24} height={24} />
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</div>
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<h3 className="text-lg font-semibold text-teal-700 leading-tight">{title}</h3>
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</div>
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<div className="relative w-full h-px bg-gray-300 mb-4 overflow-hidden">
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<div className="absolute top-0 left-0 h-full bg-gray-600 w-0 group-hover:w-full transition-all duration-500 ease-in-out"></div>
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</div>
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<p className="text-gray-600 leading-relaxed text-sm text-justify">{description}</p>
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</div>
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);
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export default function HereditaryCancerPanel() {
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const features = [
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{
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title: "Comprehensive Gene Coverage",
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desc: "Includes high- and moderate-risk genes such as BRCA1, BRCA2, TP53, MLH1, MSH2, APC, and others.",
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icon: "/images/icons/gene-coverage.png"
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},
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{
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title: "Germline Variant Detection",
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desc: "Accurately detects SNVs, Indels, and selected CNVs in genes associated with inherited cancer risk.",
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icon: "/images/icons/variant-detection.png"
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},
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{
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title: "Family-Centered Testing",
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desc: "Supports cascade testing for at-risk relatives, enabling early detection and prevention.",
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icon: "/images/icons/family-centered-testing.png"
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},
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{
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title: "Clinical Actionability",
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desc: "Provides insights that guide surveillance, preventive measures, and personalized treatment planning.",
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icon: "/images/icons/clinical-actionability.png"
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},
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{
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title: "High Sensitivity & Specificity",
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desc: "Uses ≥100X sequencing depth with ≥90% Q30 base quality for reliable variant calling.",
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icon: "/images/icons/high-sensitivity-specificity.png"
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},
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{
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title: "Expert Interpretation & Reporting",
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desc: "Variants classified using ACMG guidelines, backed by curated literature and clinical databases.",
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icon: "/images/icons/expert-interpretation-reporting.png"
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},
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{
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title: "Genetic Counseling Support",
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desc: "Optional access to pre- and post-test counseling for patient education and informed decision-making.",
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icon: "/images/icons/social-support.png"
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}
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];
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const points = [
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"About 5-10% of all cancers are linked to inherited genetic mutations, often going undetected until late stages or after multiple family members are affected.",
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"The Operify Hereditary Cancer Panel screens key high- and moderate-risk genes associated with hereditary cancer syndromes like HBOC, Lynch Syndrome (LS), Li Fraumeni Syndrome (LFS), Familial Adenomatous Polyposis (FAP), Cowden Syndrome (CS), Peutz-Jeghers Syndrome (PJS), Neurofibromatosis (NF) etc.",
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"Early identification of germline mutations enables proactive clinical decisions, including risk-reducing strategies, targeted surveillance, and family cascade testing.",
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"Studies show that genetic testing in hereditary cancer cases improves outcomes and informs care for both patients and at-risk relatives."
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];
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return (
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<section className="mx-auto px-8 pt-8">
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<h2 className="text-3xl font-bold text-teal-700 pb-2 mb-4">Operify Hereditary Cancer Panel</h2>
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<div className="mb-8">
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<ul className="space-y-4">
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{points.map((point, idx) => (
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<li key={idx} className="flex items-start">
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<span
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className="w-2 h-2 rounded-full mt-2 mr-3 flex-shrink-0"
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style={{backgroundColor: '#faae31'}}
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></span>
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<p className="text-gray-600 leading-relaxed text-base text-justify">
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{point}
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</p>
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</li>
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))}
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</ul>
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</div>
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<h3 className="text-3xl font-bold text-teal-700 mb-6 leading-tight">Key Features</h3>
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<div className="grid grid-cols-1 md:grid-cols-2 lg:grid-cols-3 gap-8">
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{features.map((feature, index) => (
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<FeatureCard
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key={index}
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icon={feature.icon}
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title={feature.title}
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description={feature.desc}
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/>
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))}
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</div>
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</section>
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);
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} |