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Written Question
22q11.2 Deletion Syndrome
Wednesday 6th March 2019

Asked by: David Duguid (Conservative - Banff and Buchan)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what assessment his Department has made of the potential effect on the public purse of adding a test for 22q11 deletion syndrome to the newborn blood spot test.

Answered by Steve Brine

No assessment has been made on adding a test for 22q11 deletion syndrome to the newborn blood spot test as the United Kingdom National Screening Committee’s (UK NSC) had not previously been asked to look at this condition.

However, as part of the UK NSC`s annual call for topics 2018, a proposal was received to consider adding the condition of 22q11 deletion syndrome (also known as DiGeorge syndrome) to the new born blood spot programme.

This is the first time the UK NSC has been asked to consider screening for 22q11. The UK NSC will be reviewing the proposal at its meeting at the end of the month and to agree next steps. Minutes of the meeting will then be published six weeks after and be made available at the following link:

https://www.gov.uk/government/groups/uk-national-screening-committee-uk-nsc


Written Question
22q11.2 Deletion Syndrome
Wednesday 6th March 2019

Asked by: David Duguid (Conservative - Banff and Buchan)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what his Department’s policy is on adding a test for 22q11 deletion syndrome to the newborn blood spot test.

Answered by Steve Brine

No assessment has been made on adding a test for 22q11 deletion syndrome to the newborn blood spot test as the United Kingdom National Screening Committee’s (UK NSC) had not previously been asked to look at this condition.

However, as part of the UK NSC`s annual call for topics 2018, a proposal was received to consider adding the condition of 22q11 deletion syndrome (also known as DiGeorge syndrome) to the new born blood spot programme.

This is the first time the UK NSC has been asked to consider screening for 22q11. The UK NSC will be reviewing the proposal at its meeting at the end of the month and to agree next steps. Minutes of the meeting will then be published six weeks after and be made available at the following link:

https://www.gov.uk/government/groups/uk-national-screening-committee-uk-nsc


Speech in Commons Chamber - Tue 27 Nov 2018
Oral Answers to Questions

"Let me start by thanking my right hon. Friend the Secretary of State for his support last Thursday on 22q Awareness Day; 22q11 deletion syndrome is second only to Down’s syndrome in its prevalence as a genetic condition, but perhaps surprisingly, there is a remarkably low level of awareness among …..."
David Duguid - View Speech

View all David Duguid (Con - Banff and Buchan) contributions to the debate on: Oral Answers to Questions

Speech in Commons Chamber - Tue 19 Jun 2018
Oral Answers to Questions

"Like many others, I welcome the announcement yesterday of the £20 billion investment in the NHS. Will my right hon. Friend join me in seeking assurances that the £2 billion extra for the Scottish Government shall be allocated to spending on the NHS in Scotland?..."
David Duguid - View Speech

View all David Duguid (Con - Banff and Buchan) contributions to the debate on: Oral Answers to Questions

Written Question
22q11.2 Deletion Syndrome
Tuesday 21st November 2017

Asked by: David Duguid (Conservative - Banff and Buchan)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health, what his policy is on (a) research into, (b) treatment of and (c) raising awareness of 22q11.2 Deletion syndrome.

Answered by Jackie Doyle-Price

22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a disorder that involves many different areas of the body and the severity can vary among patients.

The National Institute for Health Research (NIHR) and Medical Research Council support research in response to proposals from the research community and welcome high quality applications for support into any aspect of human health, including 22q11.2 deletion syndrome. These proposals are subject to peer review and judged in open competition, with awards being made on the basis of the importance of the topic to patients and health and care services, value for money and scientific quality. In all disease areas, the amount of NIHR funding depends on the volume and quality of scientific activity.

A number of United Kingdom centres contribute to active research programmes such as recently published research lead by Great Ormond Street into Thymus transplantation for complete DiGeorge syndrome. NIHR also fund relevant research at Great Ormond Street Biomedical Research Centre and the Maudsley Biomedical Research Centre.

There are 32 Immunology centres accredited including a number of paediatric immunology centres, Great Ormond Street Hospital, Newcastle Children’s Hospital, Birmingham and Manchester which provide services for these patients. These services are geographically spread out to meet the access needs of patients across the UK. Conditions such as 22q deletion syndrome are also an integral part of the immunodeficiency section of the training curriculum for paediatric and adult immunologists thus ensuring that expertise is acquired by these doctors and dispersed throughout the National Health Service.

An important landmark for patients with rare diseases was the publication of the 2013 UK Strategy for Rare Diseases to address the needs of all those affected by rare diseases. A progress report on the Strategy will be published in early 2018.