Neuropsychiatric Manifestation of Acute Intermittent Porphyria: A Case Report
Author(s) -
Tilottama Parate,
K S Tony,
Rahul D. Bhiwgade,
Faisal Pathan
Publication year - 2022
Publication title -
vidarbha journal of internal medicine
Language(s) - English
Resource type - Journals
ISSN - 0976-4356
DOI - 10.25259/vjim_10_2021
Subject(s) - porphyria , acute intermittent porphyria , medicine , polyneuropathy , disease , encephalopathy , heme , dermatology , pediatrics , psychiatry , biochemistry , chemistry , enzyme
Acute intermittent porphyria is a rare hereditary metabolic disorder with heme biosynthesis. Because of the wide and non-specific symptomatology of porphyria, diagnosis of porphyria is often missed or usually misdiagnosed as polyneuropathy or encephalopathy, or psychiatric disease. This case report is a reminder to physicians regarding porphyric neuropathy and psychiatric involvement associated with porphyria.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom