This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Pearson's marrow/pancreas syndrome

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Pearson's syndrome is caused by a sporadic insertion or deletion mutation of the mitochondrial DNA.

It is usually fatal in childhood, being characterised by:

  • pancytopaenia
  • pancreatic fibrosis
  • splenic atrophy

Patients who survive Pearson's syndrome go on to develop the Kearns-Sayre syndrome.


Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed 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.