This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

Myeloperoxidase deficiency

Authoring team

Myeloperoxidase is an enzyme stored in neutrophils and monocytes which permits the formation of highly toxic halogen-hydrogen peroxide derivatives e.g. HOCl in the presence of chloride ions. These compounds are advantageous for the destruction of phagocytosed microbes.

Myeloperoxidase deficiency is an autosomal recessive condition. As the production of hydrogen peroxide and oxygen radicals is usually unaffected, there may be no effect clinically. However, some patients are prone to recurrent and persistent bacterial infections.


Related pages

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.