Literature DB >> 29540448

Porphyria: often discussed but too often missed.

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


  8 in total

1.  Clinical Challenges of Acute Porphyria in the Young Adult.

Authors:  Shannon Burns; Allison Harmel; Sally Miller; Gabriela Figueiredo Pucci; Jonathan Greco; Michael Pulley; Michael Pizzi
Journal:  Neurohospitalist       Date:  2022-02-09

2.  A Case of MELAS With the m.3243A>G Variant of the MT-TL1 Gene Mimicking Acute Intermittent Porphyria.

Authors:  Wenjie Cai; Shilin Yang; Xiang Han
Journal:  J Clin Neurol       Date:  2022-05       Impact factor: 2.566

3.  Severe neuropathic attack in a woman with acute intermittent porphyria: a case report.

Authors:  Shiqian Huang; Ruiting Li; Yin Yuan
Journal:  J Int Med Res       Date:  2021-01       Impact factor: 1.671

4.  Patient and caregiver experiences of living with acute hepatic porphyria in the UK: a mixed-methods study.

Authors:  Liz Gill; Sue Burrell; John Chamberlayne; Stephen Lombardelli; Jordanna Mora; Nicola Mason; Marieke Schurer; Madeline Merkel; Stephen Meninger; John J Ko
Journal:  Orphanet J Rare Dis       Date:  2021-04-26       Impact factor: 4.123

5.  A draft genome assembly for the eastern fox squirrel, Sciurus niger.

Authors:  Lin Kang; Pawel Michalak; Eric Hallerman; Nancy D Moncrief
Journal:  G3 (Bethesda)       Date:  2021-12-08       Impact factor: 3.154

6.  Iron Hack - A symposium/hackathon focused on porphyrias, Friedreich's ataxia, and other rare iron-related diseases.

Authors:  Gloria C Ferreira; Jenna Oberstaller; Renée Fonseca; Thomas E Keller; Swamy Rakesh Adapa; Justin Gibbons; Chengqi Wang; Xiaoming Liu; Chang Li; Minh Pham; Guy W Dayhoff Ii; Ben Busby; Rays H Y Jiang; Linh M Duong; Luis Tañón Reyes; Luciano Enrique Laratelli; Douglas Franz; Segun Fatumo; Atm Golam Bari; Audrey Freischel; Lindsey Fiedler; Omkar Dokur; Krishna Sharma; Deborah Cragun
Journal:  F1000Res       Date:  2019-07-19

Review 7.  Genetic causes of acute encephalopathy in adults: beyond inherited metabolic and epileptic disorders.

Authors:  Dimitrios Parissis; Maria Dimitriou; Panagiotis Ioannidis
Journal:  Neurol Sci       Date:  2022-01-22       Impact factor: 3.830

Review 8.  Cutting-Edge Therapies and Novel Strategies for Acute Intermittent Porphyria: Step-by-Step towards the Solution.

Authors:  Miriam Longo; Erika Paolini; Marica Meroni; Paola Dongiovanni
Journal:  Biomedicines       Date:  2022-03-11
  8 in total

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