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EVENING TIMES – JEANS FOR GENES PROVIDES THEIR HELP TO UNIQUE HANNAH

JEANS for Genes Day on September 18 will raise vital funds for children with genetic disorders in the UK.

And two-year-old Hannah Pender, from Pollok is just one example of who the charity supports.

Hannah has an extremely rare chromosome disorder called 8p inverted duplication/deletion syndrome, which causes global developmental delays.

This means that there is an extra copy of part of the genetic material and a missing copy of another part of the genetic material on chromosome 8.

Hannah was diagnosed with the genetic condition at 20 months old but mum Rebecca Pender, 27, immediately suspected something was wrong with her first born despite doctors reassuring her Hannah was fine.

She said: “My husband John and I were really sure there was something wrong. We kept saying this to the doctors and we thought it was due to the difficult birth, but we were told she was OK.

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The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.
  • Lead with knowledge from patients. Currently, there is no cure for 8p disorders, nor is there a standard course of treatment.

The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Raise transformative funding for pioneering scientific research into treatments for a complex, rare disease involving 250+ affected genes on the short arm of the 8 th chromosome (8p). Rearrangements of these genes causes significant abnormalities to the entire neurological system, thus all organs and functions of the body– with variance in cognitive functions, gross motor skills, social development and other challenges during infancy, and throughout life;
  • Empower a unified community of 8p patients and their families so they can have meaningful lives today; and
  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.