Category : Search result: genetic heart condition


Girl, 13, completes wish list before going blind

Audrey Tyrrell, 13, is ticking off a 'visual wish list' after a diagnosis of Usher syndrome. The Essex teen aims to see the world before progressive vision loss takes hold. Read her inspiring story.

Genome Sequencing Speeds Up Rare Disease Diagnosis in Kids

A breakthrough NHS study reveals whole-genome sequencing provides diagnoses for rare genetic conditions two years earlier, offering families crucial answers and access to care. Read the inspiring story of three-year-old Nathaniel.

SADS: The silent killer claiming 500 UK lives a year

Luca Quinn's sudden death from SADS highlights this unexplained heart condition affecting 500 people annually in the UK. Discover the symptoms and support the British Heart Foundation's research.

Ex-Chelsea star Oscar diagnosed after collapsing

Former Chelsea midfielder Oscar has been diagnosed with vasovagal syncope after collapsing during pre-season tests. The Brazilian remains in hospital awaiting further cardiac examinations.

UK toddler first in world with unique genetic condition

In an extraordinary medical breakthrough, 19-month-old Oscar Sparrow from West Midlands has been identified as the only person worldwide living with a never-before-seen genetic mutation, offering new hope for rare disease research.

Daily Exercise Can Beat Heart Disease Symptoms

New research reveals how moderate daily activity can significantly reduce coronary heart disease risk and symptoms. Discover the life-changing benefits of consistent exercise for your heart health.

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