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Raouf Chorbachi, Consultant Audio-Vestibular Physician

Published: 30th September, 2019

Updated: 9th August, 2021

Author: Melanie Baldwin

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    Donate to CLEFT

    You can make a one-off donation today or sign up to giving a regular monthly gift. All donations, small or large, will help us to improve the lives of those born with cleft lip and palate both now and in the future.

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    CLEFT was established in 2007 with one aim, to help improve the lives of children born with cleft lip and palate, either by funding research into the likely causes of the condition or by helping support teams in lower and middle income countries.

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    About us

    CLEFT was established in 2007 by cleft surgeon Brian Sommerlad - based at Great Ormond Street Hospital for Children, together with a former patient and a patient's grandmother.

  • The genetics of cleft lip and palate

    The genetics of cleft lip and palate

    Investigations into the genetics of cleft lip and palate to understand more about why cleft lip and palate occurs.

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    For over 40 years, I have been involved in operating on babies, children and adults who have been born with cleft lip and/or palate.

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    Our research vision

    At CLEFT, our vision is of a future where clefts are preventable. Until we get there, we want to improve the lives of those born with cleft lip and palate.

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    Today, 1-in-700 babies in the UK are born with a cleft lip and palate, the most common form of birth defect. The impact on a child’s life as they grow is profound. Typically, they will need at least four operations. They may also require ongoing tests, treatment or therapy. It will affect the way they look but also their speech, hearing and dental development. It can leave deep psychological scars.

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