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Department of Medicine

Variegate porphyria : molecular aspects of variegate porphyria in South Africa and their biochemical and clinical consequences

Abstract

dc:description.abstract

Variegate porphyria (VP) is the clinical disorder associated with a deficiency of the haemsynthesising enzyme protoporphyrinogen oxidase (PPO). VP is one of the commonest monogenic inherited disorders in South Africa. The clinical effects include photocutaneous sensitivity and the development of potentially life-threatening acute porphyric crises. Section 1 of this dissertation examines the molecular basis for VP in South Africa.

Degree

thesis:*
Grantor dc:publisher.institution
Department of Medicine
Year dc:date.issued
2000

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Hift, R J
Advisor dc:contributor.advisor
  • Kirsch, Ralph

Rights

Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/11427/3398
OAI identifier oai:identifier
oai:open.uct.ac.za:11427/3398

Chain of custody

source
Harvested from
University of Cape Town
Base URL
open.uct.ac.za/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Hift, R J. Variegate porphyria : molecular aspects of variegate porphyria in South Africa and their biochemical and clinical consequences. Department of Medicine, 2000. http://hdl.handle.net/11427/3398