Late-onset drug-resistant epilepsy in pyridoxamine 5'-phosphate oxidase deficiency: a case report.

Autor: Naghavi E; School of Medicine, Tehran University of Medical Sciences, Tehran, Iran., Davari A; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.; Medical Colleges, Tehran University of Medical Sciences, Tehran, Iran., Bahadori AR; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.; Shiraz University of Medical Sciences, Shiraz, Iran., Razmafrooz M; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran., AmiriFard H; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran., Sabzgolin I; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran., Tafakhori A; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran., Sheikhvatan M; Medical Biology and Genetics Department, Okan University, Istanbul, Turkey.; Department of Neurology, Heidelberg University, Heidelberg, Germany., Ranji S; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran. sranji@sina.tums.ac.ir.
Jazyk: angličtina
Zdroj: Journal of medical case reports [J Med Case Rep] 2024 Nov 15; Vol. 18 (1), pp. 542. Date of Electronic Publication: 2024 Nov 15.
DOI: 10.1186/s13256-024-04876-7
Abstrakt: Background: Pyridoxamine 5'-phosphate oxidase deficiency is a rare inborn error of vitamin B 6 metabolism that presents with drug-resistant epileptic seizures. However, the condition is responsive to supplementation with the active vitamin B 6 metabolite pyridoxal 5'-phosphate and, in some cases, pyridoxine.
Case Presentation: In this case report, a 10-year-old Iranian male of Fars ethnicity came to a regional hospital in Tehran, Iran with a chief complaint of tic-like movement. He had a history of unintentional, repetitive, and stereotypic movements of both arms since the age of 4 years. The physical examination depicted facial dimorphism. During admission, the patient experienced habitual hypermotor seizures and generalized tonic-clonic seizures. Ictal electroencephalography demonstrated a generalized background attenuation and bursts of generalized, predominantly left-sided, biphasic spike-wave complexes. Whole-genome sequencing revealed a pyridoxamine 5'-phosphate oxidase deficiency as the underlying cause of the drug-resistant seizures, resulting in a low serum level of pyridoxal 5'-phosphate. The patient underwent pyridoxine supplementation therapy, which ultimately resolved his seizures. At 6 months, he was seizure free.
Conclusion: Physicians ought to be aware of manifestations of vitamin B6 deficiency such as mimicking tic and consider it in the differential for drug-resistant epilepsy.
Competing Interests: Declarations Ethics approval and consent to participate Informed consent was obtained from the participant and the parents of the patient included in the study. Consent for publication Written informed consent was obtained from the patient’s legal guardian for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal. Competing interests The authors declare that they have no competing interests.
(© 2024. The Author(s).)
Databáze: MEDLINE
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