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Porphyria: often discussed but too often missed
Ronan O'Malley1,2, Ganesh Rao2,3, Penelope Stein4
1Department of Neurology, Sheffield Teaching Hospitals (STH), Sheffield, UK.
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.
Insights
Acute intermittent porphyria (AIP) is a frequently missed diagnosis that causes varied neurological symptoms. Early recognition and management of AIP are crucial to prevent severe patient outcomes.
Area of Science:
- Biochemistry
- Genetics
- Neurology
Background:
- Acute intermittent porphyria (AIP) is a rare genetic disorder often overlooked in clinical practice.
- AIP can manifest with a wide range of neurological symptoms, leading to diagnostic delays.
- Misdiagnosis or delayed diagnosis of AIP can result in severe and potentially irreversible complications.
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