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28 November 2024
AI for rare disease: accelerating drug repurposing and diagnosis.

As the complexity of rare diseases continues to challenge traditional treatment and diagnostic methods, artificial intelligence (AI) is emerging as a transformative tool. It enables the repurposing of existing drugs for rare disease treatments and offers faster, more accurate diagnoses for patients. In this blog, we explore the evolving role of AI in drug repurposing […]

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19 June 2024
Rare disease across the globe – differences in approaches.

In our last rare disease blog, we explored how a patient-centric approach can better equip healthcare professionals (HCPs) to guide patients on their rare disease journey. In our latest blog, we review how approaches to rare disease differ across the globe, the impact that this has on patients, and how better awareness of rare conditions […]

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21 May 2024
Misdiagnosed and misunderstood: the benefits of a patient-centric approach for rare disease.

In our previous rare disease blog, we explored the advancements in genetic sequencing and how it is revolutionising research in this field. We also discussed the exciting possibilities it brings for diagnosis and treatment methods. In this blog, we will take a look at how treatments of rare conditions can be personalised beyond genetics and […]

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21 April 2024
Putting rare disease under the microscope: why a deeper understanding of genetics counts.

Our genetic makeup has a significant role in health and disease. In this blog, we will explore how well we understand the genetic components of rare disease, and what is being done to improve diagnosis and treatment outcomes for patients.

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28 February 2023
Infographic – the rare disease patient journey.

For Rare Disease Awareness Day 2023, the IGNIFI team wanted to highlight the difficulties faced by the 300 million people worldwide living with a rare disease.1 Like their disease, the patient journey of those living with a rare health condition is rarely straightforward. Take a look at our interactive infographic to view their challenges from symptoms […]

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10 June 2022
How whole genome sequencing is revolutionising the rare disease patient experience.

As mentioned in our Rare Disease Day blog earlier this year, whole genome sequencing (WGS) projects and the data sets they produce are paving the way for developments in research, diagnosis, and early interventions for rare diseases. Since the Human Genome Project was completed in 2003,1 sequencing techniques have progressed in leaps and bounds, increasing […]

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3 March 2022
Improving healthcare for rare disease patients.

There are thought to be around 300 million people worldwide living with a rare disease at any given time.1 While their conditions and symptoms will vary, many aspects of their experience are shared. Following on from Rare Disease Day 2022, we decided to take a deeper look into the patient journey of those living with a […]

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