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Case ReportCase Report
Open Access

Encephalopathy mimicking non-convulsive status Epilepticus

Ramachandiran Nandhagopal, Fathiya Al-Murshedi, Mujahid Al-Busaidi and Amna Al-Busaidi
Neurosciences Journal January 2018, 23 (1) 52-56; DOI: https://doi.org/10.17712/nsj.2018.1.20170214
Ramachandiran Nandhagopal
From the Neurology unit (Nandhagopal), Department of Medicine, Internal Medicine (Al-Busaidi), Genetic and Developmental Medicine Clinic (Al-Murshedi), College of Medicine and Health Sciences, Muscat, Oman and Oman Medical Specialty Board (Al-Busaidi A), Internal Medicine Residency Program, Oman
DM, FRCP
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  • For correspondence: [email protected]
Fathiya Al-Murshedi
From the Neurology unit (Nandhagopal), Department of Medicine, Internal Medicine (Al-Busaidi), Genetic and Developmental Medicine Clinic (Al-Murshedi), College of Medicine and Health Sciences, Muscat, Oman and Oman Medical Specialty Board (Al-Busaidi A), Internal Medicine Residency Program, Oman
MD, FRCPC
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Mujahid Al-Busaidi
From the Neurology unit (Nandhagopal), Department of Medicine, Internal Medicine (Al-Busaidi), Genetic and Developmental Medicine Clinic (Al-Murshedi), College of Medicine and Health Sciences, Muscat, Oman and Oman Medical Specialty Board (Al-Busaidi A), Internal Medicine Residency Program, Oman
MD, FRCPC
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Amna Al-Busaidi
From the Neurology unit (Nandhagopal), Department of Medicine, Internal Medicine (Al-Busaidi), Genetic and Developmental Medicine Clinic (Al-Murshedi), College of Medicine and Health Sciences, Muscat, Oman and Oman Medical Specialty Board (Al-Busaidi A), Internal Medicine Residency Program, Oman
MD
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    Figure 1

    Timeline picture of the clinical course of Patient #1(a 30-year-old woman) with hyperammonemic encephalopathy mimicking non-convulsive status epilepticus

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    Figure 2

    EEG obtained during an unresponsive episode (A) in a 30-year-old woman (Patient# 1) showed continuous, frontally dominant, generalized, 2.5 Hz sharp and wave discharges, with a triphasic morphology in some channels (e.g., Fz-Cz). Following intravenous administration of diazepam (B), there was complete resolution of this pattern, with the appearance of diffuse slowing in the theta range and movement artefacts (patient opened her eyes and withdrew her limbs to painful stimuli and then sat up in the bed and attempted to remove the electrodes) indicating arousal. (Low-frequency filter 0.3 Hz, high-frequency filter 50 Hz).

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    Figure 3

    Marked worsening of hyperammonemia in relation to carbohydrate infusion that was provided as part of the standard treatment protocol for episodic hyperammonemic encephalopathy (mimicking non-convulsive status epilepticus) in a previously undiagnosed case (patient#1) of adult-onset citrullinemia. The plasma glucose and lactate values are in mmol/l.

  • Figure 4
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    Figure 4

    Timeline picture of the clinical course of Patient #2 (a 19-year-old man) with hyperammonemic encephalopathy mimicking non-convulsive status epilepticus

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    Figure 5

    EEG obtained during an episode of hyperammonemic encephalopathy (A) with a plasma ammonia level of 105 µmol/l in a 19-year-old man (patient# 2) with a known diagnosis of arginase deficiency showed continuous, frontally dominant, generalized, 2.5 Hz sharp and wave discharges, similar to Figure 1A. Twenty hours following the standard treatment protocol for hyperammonemia that included infusion of dextrose and ammonia scavenger (B), he was conscious and alert and the corresponding EEG normalized to a posterior dominant alpha background rhythm without any ictal discharges. (Low-frequency filter 1 Hz, high-frequency filter 70 Hz).

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Neurosciences Journal: 23 (1)
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Encephalopathy mimicking non-convulsive status Epilepticus
Ramachandiran Nandhagopal, Fathiya Al-Murshedi, Mujahid Al-Busaidi, Amna Al-Busaidi
Neurosciences Journal Jan 2018, 23 (1) 52-56; DOI: 10.17712/nsj.2018.1.20170214

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Encephalopathy mimicking non-convulsive status Epilepticus
Ramachandiran Nandhagopal, Fathiya Al-Murshedi, Mujahid Al-Busaidi, Amna Al-Busaidi
Neurosciences Journal Jan 2018, 23 (1) 52-56; DOI: 10.17712/nsj.2018.1.20170214
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