Immundefizienz 26 mit oder ohne neurologische Anomalien

Last updated on: 30.05.2022

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

DefinitionThis section has been translated automatically.

Very rare immunodeficiency syndrome characterized by a mutation in the DNA-PKcs gene that presents as a classic SCID syndrome. Patients with this mutation do not differ from patients with a recombination activating gene or Artemis deficiency (van der Burg M et al. 2009).

Last updated on: 30.05.2022