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Image Description: Brown & Cream Coloured Image Depicting a Typewriter With Wording "Rare Genetic Disorder" Typed On Paper. Image Credit: PhotoFunia.com Category: Vintage Typewriter.

A Three-Year-Old Receives Groundbreaking Gene Therapy

In a historic medical breakthrough, a three-year-old child has become the youngest patient ever to receive a revolutionary form of gene therapy, offering hope to families affected by rare and life-threatening genetic conditions. The pioneering treatment, administered at a leading children’s hospital in the UK, has shown early signs of success and could change the trajectory of treatment for similar disorders worldwide.

Cell & Gene Therapy Text On Typewriter Paper. Image Credit: PhotoFunia.com

Synthetic Futures or Superhuman Fears? The Genetic Frontier Stirring Global Debate

A groundbreaking and highly controversial scientific initiative is now underway in the UK, as leading British researchers aim to synthesize the first human genome entirely from scratch, not by altering existing DNA, but by building it letter by letter in the lab. Spearheaded by scientists from the University of Oxford, Cambridge, Kent, Manchester, and Imperial College London, this ambitious project is known as the Synthetic Human Genome (SynHG) project and is being funded by the Wellcome Trust, the world’s largest medical research charity.

AI Bot

The Transformative Impact of AI On Disabled Entrepreneurs

The fear that AI could be a competitor arises from concerns about job displacement, reduced creativity, and economic disruption. However, AI’s true potential lies in being a co-creator, enabling individuals, including disabled entrepreneurs, to leverage its capabilities to enhance and accelerate their work, while still maintaining the human touch in decision-making, creativity, and empathy.

Black & Gray Stethoscope

30 Healthcare Trends to Watch in 2025

AI is set to transform healthcare by reducing the need for patients to phone or physically visit clinics for consultations. Tools such as those can be potentially offered on the domain GPAI.co.uk enable fully digital interactions across various sectors, including government and healthcare.

Patau Syndrome: Understanding a Rare Genetic Disorder

Patau Syndrome, also known as Trisomy 13, is a rare genetic disorder caused by the presence of an extra copy of chromosome 13 in some or all of the body’s cells. This condition leads to severe intellectual disability and physical abnormalities, including heart defects, brain or spinal cord abnormalities, very small or poorly developed eyes, extra fingers or toes, an opening in the lip (cleft lip) with or without an opening in the roof of the mouth (cleft palate), and weak muscle tone (hypotonia).