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SMS Foundation UK

Supporting SMS families for a positive future

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We are a small charity that supports families living with Smith-Magenis syndrome (SMS)

Never feel isolated or alone. Call our helpline and leave a message: 0300 101 0034 (we aim to respond to messages within 48 hours).

Newly Diagnosed?

Scientific Papers

September 12, 2023

The latest information from SMS Foundation UK is stored here and continually updated as we produce additional information.

Living with SMS

This information was collated with SMS by experts in Smith-Magenis Syndrome or medical professionals working with an individual with SMS. It identifies the monitoring required in each medical area and the reasoning for the requirement.

Download Managing children and adults with SMS

Technical Papers

Practical Genetics by Dr Sarah Elsea

A scientific article, providing in depth and detailed information about the genetics of SMS. Looking sat the RAI1 gene and the implications of it.

Download Practical Genetics by Dr Sarah Elsea

Smith-Magenis Syndrome by Dr Orlee Udwin

A summary of a medical paper focussed on SMS – written by our Chair of professionals.

Download SMS by Dr Orlee Udwin

Williams / SMS by Orlee Udwin

An article discussing and comparing the rare genetic syndromes – Williams and Smith-Magenis.

Download Williams and SMS

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Never feel isolated or alone. Call our helpline: 0300 101 0034

Please note: This is an answer phone service that will alert us as soon as a message is left. A member of the team will call you back as soon as possible – we aim to respond to messages within 48 hours.

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