Health page creation
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app/health/rare-disorders/components/WESInfo.jsx
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app/health/rare-disorders/components/WESInfo.jsx
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export default function WESInfo() {
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return (
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<section className="mx-auto px-10 pt-12">
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<h2 className="text-2xl font-semibold text-gray-700 text-left pb-2 mb-4">
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Who Should Consider Whole Exome Sequencing (WES)?
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</h2>
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<p className="text-gray-600 leading-relaxed text-base mb-4 text-justify">
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Whole Exome Sequencing (WES) is recommended for individuals with unexplained genetic
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disorders, complex or atypical clinical presentations, or when prior genetic tests
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have been inconclusive.
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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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It is especially valuable in diagnosing rare inherited diseases, uncovering the cause
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of developmental delays, intellectual disabilities, or early-onset neurological
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conditions, and providing insights for personalized treatment planning.
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</p>
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<p className="text-gray-600 leading-relaxed text-base text-justify">
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WES can help identify genetic causes in a wide range of rare disorders.
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</p>
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</section>
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);
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}
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