This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Porphyria cutanea tarda (PCT)

Authoring team

Porphyria cutanea tarda may inherited (autosomal dominant) but is commonly an acquired disorder of porphyrin metabolism.

There is a deficiency in uroporphyrinogen decarboxylase (chromosome 1p34) which results in:

  • bullous reaction to sunlight
  • hyperpigmentation and scarring
  • liver disease

Porphyria cutanea tarda usually presents in middle and old age.


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.