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fix: several typos in NESTOR app #5032

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Merged
merged 1 commit into from
May 9, 2025
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fix: several typos in NESTOR app #5032

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12 changes: 6 additions & 6 deletions apps/nestor-public/src/pages/view-about.vue
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Original file line number Diff line number Diff line change
@@ -1,19 +1,19 @@
<template>
<Page>
<PageHeader
title="NESTOR Resgistry"
subtitle="About the NESTOR registry"
title="NESTOR Registry"
subtitle="About the NESTOR Registry"
titlePositionX="center"
titlePositionY="center"
height="medium"
/>
<PageSection aria-labelledby="about-us-section-title">
<h2 id="about-us-section-title">About the NESTOR registry</h2>
<h2 id="about-us-section-title">About the NESTOR Registry</h2>
<p>
The NESTOR registry is a web-based platform that facilitates and
The NESTOR Registry is a web-based platform that facilitates and
accelerates research to improve diagnostics, treatment and the provision
of high-quality healthcare for patients with one of rare genetic tumor
risk syndromes. The NESTOR registry is affiliated to the KWF NESTOR
of high-quality healthcare for patients with one of rare genetic tumour
risk syndromes. The NESTOR Registry is affiliated to the KWF NESTOR
project.
</p>
<MessageBox type="warning">
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6 changes: 3 additions & 3 deletions apps/nestor-public/src/pages/view-home.vue
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Original file line number Diff line number Diff line change
Expand Up @@ -25,7 +25,7 @@
genetic tumour risk syndromes (genturis). It is associated with 8 Dutch
centres participating in the KWF NESTOR project and serves as a
comprehensive resource for all patients with one of the rare genetic
tumor risk syndromes.
tumour risk syndromes.
</p>
</PageSection>
<PageSection
Expand Down Expand Up @@ -75,7 +75,7 @@
<p>
Therefore the primary aim of the NESTOR Registry is to support research
that provides valuable insights into the natural history of rare genetic
tumor risk syndromes and the care pathway for affected patients. By
tumour risk syndromes and the care pathway for affected patients. By
collecting data from a large cohort of affected patients, the registry
will enable regulated data access according to a defined data access
policy.
Expand Down Expand Up @@ -107,7 +107,7 @@
</li>
<li>
Accelerating collaborative research efforts to generate new knowledge
on rare genetic tumor risk syndromes
on rare genetic tumour risk syndromes
</li>
</ul>
</PageSection>
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