Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy

Metabolic strokes are a notable feature associated with acute catabolic crises in patients with propionic acidemia. Despite their importance, these events are not well characterized. Here, we present the clinical history of a patient with propionic acidemia who developed 5 episodes of acute hemipare...

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Main Authors: Mohammed Almuqbil MD, FRCPC, Jeffrey M. Chinsky MD, PhD, Siddharth Srivastava MD
Format: Article
Language:English
Published: SAGE Publishing 2019-09-01
Series:Child Neurology Open
Online Access:https://doi.org/10.1177/2329048X19873242
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spelling doaj-6b61f3d30c4b490fae22bf1edd1c03e82020-11-25T03:46:39ZengSAGE PublishingChild Neurology Open2329-048X2019-09-01610.1177/2329048X19873242Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without EncephalopathyMohammed Almuqbil MD, FRCPC0Jeffrey M. Chinsky MD, PhD1Siddharth Srivastava MD2 King Abdullah International Medical Research Center, King Abdullah Specialist Children’s Hospital—Ministry of National Guard, Riyadh, Saudi Arabia Department of Pediatrics, Johns Hopkins Hospital, Baltimore, MD, USA Department of Neurology, Boston Children’s Hospital, Boston, MA, USAMetabolic strokes are a notable feature associated with acute catabolic crises in patients with propionic acidemia. Despite their importance, these events are not well characterized. Here, we present the clinical history of a patient with propionic acidemia who developed 5 episodes of acute hemiparesis between 3 and 11 years of age. The clinical finding of hemiparesis associated with 4 of these 5 events were shorted lived (2-5 days). Neuroimaging showed signal changes in the basal ganglia manifesting many years following the initial episode. Two of the episodes were accompanied by definite seizures. Based on these factors, the hemiparetic events were most consistent with metabolic strokes, though what is distinctive is that most of the events occurred without evidence of metabolic decompensation; brain magnetic resonance imaging findings were not suggestive in the acute setting. We present a framework for evaluating suspected metabolic stroke in propionic acidemia, in light of the sometimes perplexing clinical heterogeneity underlining these events.https://doi.org/10.1177/2329048X19873242
collection DOAJ
language English
format Article
sources DOAJ
author Mohammed Almuqbil MD, FRCPC
Jeffrey M. Chinsky MD, PhD
Siddharth Srivastava MD
spellingShingle Mohammed Almuqbil MD, FRCPC
Jeffrey M. Chinsky MD, PhD
Siddharth Srivastava MD
Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy
Child Neurology Open
author_facet Mohammed Almuqbil MD, FRCPC
Jeffrey M. Chinsky MD, PhD
Siddharth Srivastava MD
author_sort Mohammed Almuqbil MD, FRCPC
title Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy
title_short Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy
title_full Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy
title_fullStr Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy
title_full_unstemmed Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy
title_sort metabolic strokes in propionic acidemia: transient hemiplegic events without encephalopathy
publisher SAGE Publishing
series Child Neurology Open
issn 2329-048X
publishDate 2019-09-01
description Metabolic strokes are a notable feature associated with acute catabolic crises in patients with propionic acidemia. Despite their importance, these events are not well characterized. Here, we present the clinical history of a patient with propionic acidemia who developed 5 episodes of acute hemiparesis between 3 and 11 years of age. The clinical finding of hemiparesis associated with 4 of these 5 events were shorted lived (2-5 days). Neuroimaging showed signal changes in the basal ganglia manifesting many years following the initial episode. Two of the episodes were accompanied by definite seizures. Based on these factors, the hemiparetic events were most consistent with metabolic strokes, though what is distinctive is that most of the events occurred without evidence of metabolic decompensation; brain magnetic resonance imaging findings were not suggestive in the acute setting. We present a framework for evaluating suspected metabolic stroke in propionic acidemia, in light of the sometimes perplexing clinical heterogeneity underlining these events.
url https://doi.org/10.1177/2329048X19873242
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