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PUBLIC RELEASE DATE:
24-Jan-2014

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Contact: Alison Barbuti
alison.barbuti@manchester.ac.uk
44-016-127-58383
University of Manchester

Cause identified for children and adults with joint, skeletal and skin problems

Scientists from the University of Manchester and Central Manchester University Hospitals NHS Foundation Trust have identified the cause of a rare condition called Leri's pleonosteosis

Scientists from The University of Manchester and Central Manchester University Hospitals NHS Foundation Trust have identified the cause of a rare condition called Leri's pleonosteosis (LP).

Dr Sid Banka from the Manchester Centre for Genomic Medicine at The University of Manchester, led a team of researchers on the study which was published in Annals of Rheumatic Diseases journal Jan. 18, 2014.

LP is an inherited condition in which children are born with contractures of multiple joints and then develop difficulty of joint movements that progress in severity with age. The research team showed that extra genetic material on chromosome number 8 caused the condition in two families from Manchester.

Some patients with LP also develop thickening of their skin, similar to that seen in patients with a more common disorder called scleroderma.

Using their new knowledge, the research team showed that the genetic cause of LP is linked to whether people get scleroderma or not.

This work opens opportunities to understand scleroderma and explore new treatments.

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