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Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies

Recruiting
years of age
Both
Phase N/A

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Overview

Individuals with suspected primary immunodeficiency will be studied and the results compared with healthy controls. Primary immunodeficiency may manifest as recurrent, severe or unusual infections as well as signs and symptoms of immune dysregulation such as autoimmunity or lymphoproliferation.

Description

Patients with a suspected immunodeficiency will be identified and invited to participate. Upon agreement, an additional blood sample will be collected when they have their routine bloods taken. If the study participants undergoes anaesthesia for any other reason, a small skin biopsy will be taken as well. Additional samples including blood samples or mouth swabs will be taken from healthy family members. Blood from healthy controls will only be taken when there is a clinical need for blood sampling (or when the study participant is already anaesthetised for any other reason) and not for research purposes only.

Eligibility

Inclusion Criteria:

  • Patient with suspected PID, healthy relative or healthy volunteer
  • consent

Exclusion Criteria:

  • none

Study details

Immunologic Deficiency Syndromes

NCT02735824

University Children's Hospital, Zurich

26 January 2024

Step 1 Get in touch with the nearest study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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