Health page creation

app/health/oncology/Components/CancerKeyFeatures.jsx

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+export default function CancerKeyFeatures() {
+  const features = [
+    { title: "Comprehensive Gene Coverage", desc: "Includes high- and moderate-risk genes such as BRCA1, BRCA2, TP53, MLH1, MSH2, APC, and others." },
+    { title: "Germline Variant Detection", desc: "Accurately detects SNVs, Indels, and selected CNVs in genes associated with inherited cancer risk." },
+    { title: "Family-Centered Testing", desc: "Supports cascade testing for at-risk relatives, enabling early detection and prevention." },
+    { title: "Clinical Actionability", desc: "Provides insights that guide surveillance, preventive measures, and personalized treatment planning." },
+    { title: "High Sensitivity & Specificity", desc: "Uses ≥100X sequencing depth with ≥90% Q30 base quality for reliable variant calling." },
+    { title: "Expert Interpretation & Reporting", desc: "Variants classified using ACMG guidelines, backed by curated literature and clinical databases." },
+    { title: "Genetic Counseling Support", desc: "Optional access to pre- and post-test counseling for patient education and informed decision-making." }
+  ];
+
+  return (
+    <section className="p-10">
+      <h3 className="text-lg font-semibold mb-4">Key Features</h3>
+      <div className="grid md:grid-cols-2 gap-4">
+        {features.map((f, idx) => (
+          <div key={idx} className="border p-4 rounded-lg hover:shadow-lg transition-shadow">
+            <h4 className="font-semibold">{f.title}</h4>
+            <p className="text-gray-600">{f.desc}</p>
+          </div>
+        ))}
+      </div>
+    </section>
+  );
+}

app/health/oncology/Components/HereditaryCancerPanel.jsx

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

app/health/oncology/Components/OncologyIntro.jsx

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+export default function OncologyIntro() {
+  return (
+    <section className="mx-auto px-10 pt-12">
+      <h1 className="text-4xl font-bold text-gray-700 text-left pb-2 mb-4">Oncology</h1>
+      <h2 className="text-2xl font-semibold text-gray-700 mb-4">Turning Complexity into Clarity</h2>
+      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+        Cancer is not a single disease—it's a highly complex and dynamic group of disorders, 
+        often driven by a multitude of genomic alterations. Despite advancements in treatment, 
+        many patients still face uncertainty due to incomplete or delayed molecular diagnoses.
+      </p>
+      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+        At Operify Health, we recognize that behind every tumor is a unique genetic story waiting 
+        to be told. Our precision oncology solutions utilize high-throughput Next Generation 
+        Sequencing (NGS) to analyze both somatic and germline mutations—providing clinicians 
+        with actionable insights that inform targeted therapies, immunotherapy decisions, and 
+        hereditary cancer risk assessments.
+      </p>
+      <p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
+        This genomic-driven approach is especially critical in advanced and treatment-resistant 
+        cancers, where conventional methods often fall short. Studies have shown that integrating 
+        broad-panel NGS into cancer care can impact clinical decision-making in up to 30% of cases, 
+        leading to more personalized and effective treatment strategies.
+      </p>
+      <p className="text-gray-600 leading-relaxed text-base text-justify">
+        By combining cutting-edge sequencing, advanced bioinformatics, and curated clinical evidence, 
+        Operify Health empowers oncologists to move from uncertainty to precision—ensuring every cancer 
+        patient's care is as individualized as their diagnosis.
+      </p>
+    </section>
+  );
+}

app/health/oncology/Components/OncologyTitle.jsx

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+import React from 'react';
+
+const OncologyTitle = () => {
+  return (
+    <section 
+      className="relative bg-cover bg-center py-6 h-24" 
+      style={{ backgroundImage: "url('/images/bredcrumb.jpg')" }}
+    >
+      {/* Breadcrumb */}
+      <div className="relative z-10 mb-1 -mt-3">
+        <div className="container mx-auto max-w-none px-4">
+          <nav className="flex items-center space-x-2 text-sm">
+            <a href="/" className="text-white hover:text-yellow-400 underline">Home</a>
+            <span className="text-white">
+              <svg className="w-3 h-3" fill="currentColor" viewBox="0 0 20 20">
+                <path fillRule="evenodd" d="M7.293 14.707a1 1 0 010-1.414L10.586 10 7.293 6.707a1 1 0 011.414-1.414l4 4a1 1 0 010 1.414l-4 4a1 1 0 01-1.414 0z" clipRule="evenodd" />
+              </svg>
+            </span>
+            <a href="/about-us" className="text-white hover:text-yellow-400 underline">Health</a>
+            <span className="text-white">
+              <svg className="w-3 h-3" fill="currentColor" viewBox="0 0 20 20">
+                <path fillRule="evenodd" d="M7.293 14.707a1 1 0 010-1.414L10.586 10 7.293 6.707a1 1 0 011.414-1.414l4 4a1 1 0 010 1.414l-4 4a1 1 0 01-1.414 0z" clipRule="evenodd" />
+              </svg>
+            </span>
+            <span className="text-white">Oncology</span>
+          </nav>
+        </div>
+      </div>
+      
+      {/* Page Title */}
+      <div className="relative z-10 text-center -mt-2">
+        <h1 className="text-4xl md:text-4xl font-bold text-white mb-2">
+          Oncology
+        </h1>
+        <div className="w-16 h-1 bg-yellow-400 mx-auto"></div>
+      </div>
+    </section>
+  );
+};
+
+export default OncologyTitle;

app/health/oncology/Components/SampleRequirements.jsx

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+export default function SampleRequirements({ title, items }) {
+  return (
+    <section className="p-8">
+      <h3 className="text-lg font-semibold mb-4">Sample Requirements – {title}</h3>
+      <ul className="list-disc list-inside text-gray-700 space-y-2">
+        {items.map((item, idx) => (
+          <li key={idx}>{item}</li>
+        ))}
+      </ul>
+    </section>
+  );
+}

app/health/oncology/page.js

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+import OncologyTitle from './components/OncologyTitle';
+import OncologyIntro from './components/OncologyIntro';
+import HereditaryCancerPanel from './components/HereditaryCancerPanel';
+import SampleRequirements from '../rare-disorders/components/SampleRequirements';
+
+import PageLayout from '../../components/Layout/PageLayout';
+
+export default function OncologyPage() {
+
+  return (
+    <PageLayout fixedHeader={true}>
+      {/* Page Title */}
+      <OncologyTitle />
+
+      {/* Intro */}
+      <OncologyIntro />
+
+      {/* Hereditary Cancer Panel */}
+      <HereditaryCancerPanel />
+
+      
+
+      {/* Sample Requirements */}
+      <SampleRequirements/>
+    </PageLayout>
+  );
+}