Files
operify/app/health/rare-disorders/components/WESInfo.jsx
2025-08-12 11:50:37 +05:30

22 lines
1.1 KiB
JavaScript

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