| Literature DB >> 29540448 |
Ronan O'Malley1,2, Ganesh Rao2,3, Penelope Stein4, Oliver Bandmann1,2.
Abstract
The diagnosis of acute intermittent porphyria (AIP) is often overlooked. We describe a patient with this condition who had all the 'bells and whistles', in whom the diagnosis was only made after considerable delay. Far from an esoteric condition haunting examination candidates, AIP is an important cause of a broad spectrum of neurological symptoms. Its early recognition allows the astute clinician to prevent potentially devastating sequelae. We provide practical guidance on the investigation and management of this complex disorder. With a 'back to basics' approach to the underlying genetics and biochemistry, we hope to dispel some of the confusion that may obstruct a timely diagnosis. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: neuropathy; porphyria
Mesh:
Year: 2018 PMID: 29540448 DOI: 10.1136/practneurol-2017-001878
Source DB: PubMed Journal: Pract Neurol ISSN: 1474-7758