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Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature
Objective: Childhood seizures have various nonneurological etiologies. The patient’s magnesium levels should be measured when evaluating afebrile seizures. The purpose of the current case series is to describe a systematic approach for diagnosing hypomagnesemia using 3 recent patient cases. Methods:...
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Published in: | Child neurology open 2016-01, Vol.3, p.2329048X16674834-2329048X16674834 |
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container_end_page | 2329048X16674834 |
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container_start_page | 2329048X16674834 |
container_title | Child neurology open |
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creator | Chen, Becky Biqi Prasad, Chitra Kobrzynski, Marta Campbell, Craig Filler, Guido |
description | Objective:
Childhood seizures have various nonneurological etiologies. The patient’s magnesium levels should be measured when evaluating afebrile seizures. The purpose of the current case series is to describe a systematic approach for diagnosing hypomagnesemia using 3 recent patient cases.
Methods:
This case series describes 3 patients with unprovoked hypomagnesemia-associated seizures. The authors describe the differential diagnosis, pathophysiology, and the workup of hypomagnesemia-associated seizures.
Results:
Hypomagnesemia contributed to the cause of the seizures in all 3 cases. Various causes of hypomagnesemia were investigated, including genetic etiologies. All 3 patients were maintained at a magnesium level >0.65 mmol/L, which improved or eliminated the seizures.
Significance:
Magnesium levels should always be measured when trying to determine the etiology of seizures. Hypomagnesemia and afebrile seizures should be treated with the goal of maintaining a magnesium concentration >0.65 mmol/L. Although rare, genetic causes of hypomagnesemia should be considered, once common causes of hypomagnesemia are ruled out. |
doi_str_mv | 10.1177/2329048X16674834 |
format | article |
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Childhood seizures have various nonneurological etiologies. The patient’s magnesium levels should be measured when evaluating afebrile seizures. The purpose of the current case series is to describe a systematic approach for diagnosing hypomagnesemia using 3 recent patient cases.
Methods:
This case series describes 3 patients with unprovoked hypomagnesemia-associated seizures. The authors describe the differential diagnosis, pathophysiology, and the workup of hypomagnesemia-associated seizures.
Results:
Hypomagnesemia contributed to the cause of the seizures in all 3 cases. Various causes of hypomagnesemia were investigated, including genetic etiologies. All 3 patients were maintained at a magnesium level >0.65 mmol/L, which improved or eliminated the seizures.
Significance:
Magnesium levels should always be measured when trying to determine the etiology of seizures. Hypomagnesemia and afebrile seizures should be treated with the goal of maintaining a magnesium concentration >0.65 mmol/L. Although rare, genetic causes of hypomagnesemia should be considered, once common causes of hypomagnesemia are ruled out.</description><identifier>ISSN: 2329-048X</identifier><identifier>EISSN: 2329-048X</identifier><identifier>DOI: 10.1177/2329048X16674834</identifier><identifier>PMID: 28503619</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Original</subject><ispartof>Child neurology open, 2016-01, Vol.3, p.2329048X16674834-2329048X16674834</ispartof><rights>The Author(s) 2016</rights><rights>The Author(s) 2016 2016 SAGE Publications</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1904-3d1d1ab85d989900bc6ab95dd017900b1c84bdb885ccfe056de0857577b3a353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417264/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417264/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,21945,27830,27901,27902,36990,44921,45309,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28503619$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Becky Biqi</creatorcontrib><creatorcontrib>Prasad, Chitra</creatorcontrib><creatorcontrib>Kobrzynski, Marta</creatorcontrib><creatorcontrib>Campbell, Craig</creatorcontrib><creatorcontrib>Filler, Guido</creatorcontrib><title>Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature</title><title>Child neurology open</title><addtitle>Child Neurol Open</addtitle><description>Objective:
Childhood seizures have various nonneurological etiologies. The patient’s magnesium levels should be measured when evaluating afebrile seizures. The purpose of the current case series is to describe a systematic approach for diagnosing hypomagnesemia using 3 recent patient cases.
Methods:
This case series describes 3 patients with unprovoked hypomagnesemia-associated seizures. The authors describe the differential diagnosis, pathophysiology, and the workup of hypomagnesemia-associated seizures.
Results:
Hypomagnesemia contributed to the cause of the seizures in all 3 cases. Various causes of hypomagnesemia were investigated, including genetic etiologies. All 3 patients were maintained at a magnesium level >0.65 mmol/L, which improved or eliminated the seizures.
Significance:
Magnesium levels should always be measured when trying to determine the etiology of seizures. Hypomagnesemia and afebrile seizures should be treated with the goal of maintaining a magnesium concentration >0.65 mmol/L. Although rare, genetic causes of hypomagnesemia should be considered, once common causes of hypomagnesemia are ruled out.</description><subject>Original</subject><issn>2329-048X</issn><issn>2329-048X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><recordid>eNp1UM9LwzAYDaK4MXf3JMOTl2rSNE16EWSoEwaC7uAtpMm32dE2NWmF-debsjmm4On79b73Hg-hc4KvCeH8JqZxhhPxRtKUJ4ImR2jYr6J-d3zQD9DY-zXGmHDKszg9RYNYMExTkg3R5SsUX50DP3mBUrVgJq2dzDaNrdSqBg9Voc7QyVKVHsa7OkKLh_vFdBbNnx-fpnfzSJPgI6KGGKJywUwmsgzjXKcqz5gxQbcfiRZJbnIhmNZLwCw1gAXjjPOcKsroCN1uaZsur8BoqFunStm4olJuI60q5O9LXbzLlf2ULCE8TpNAcLUjcPajA9_KqvAaylLVYDsvSbBFCAtSAYq3UO2s9w6WexmCZR-u_BtueLk4tLd_-IkyAKItwKsVyLXtXB3S-p_wG_PFgTA</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Chen, Becky Biqi</creator><creator>Prasad, Chitra</creator><creator>Kobrzynski, Marta</creator><creator>Campbell, Craig</creator><creator>Filler, Guido</creator><general>SAGE Publications</general><scope>AFRWT</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201601</creationdate><title>Seizures Related to Hypomagnesemia</title><author>Chen, Becky Biqi ; Prasad, Chitra ; Kobrzynski, Marta ; Campbell, Craig ; Filler, Guido</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1904-3d1d1ab85d989900bc6ab95dd017900b1c84bdb885ccfe056de0857577b3a353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Becky Biqi</creatorcontrib><creatorcontrib>Prasad, Chitra</creatorcontrib><creatorcontrib>Kobrzynski, Marta</creatorcontrib><creatorcontrib>Campbell, Craig</creatorcontrib><creatorcontrib>Filler, Guido</creatorcontrib><collection>SAGE Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Child neurology open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Becky Biqi</au><au>Prasad, Chitra</au><au>Kobrzynski, Marta</au><au>Campbell, Craig</au><au>Filler, Guido</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature</atitle><jtitle>Child neurology open</jtitle><addtitle>Child Neurol Open</addtitle><date>2016-01</date><risdate>2016</risdate><volume>3</volume><spage>2329048X16674834</spage><epage>2329048X16674834</epage><pages>2329048X16674834-2329048X16674834</pages><issn>2329-048X</issn><eissn>2329-048X</eissn><abstract>Objective:
Childhood seizures have various nonneurological etiologies. The patient’s magnesium levels should be measured when evaluating afebrile seizures. The purpose of the current case series is to describe a systematic approach for diagnosing hypomagnesemia using 3 recent patient cases.
Methods:
This case series describes 3 patients with unprovoked hypomagnesemia-associated seizures. The authors describe the differential diagnosis, pathophysiology, and the workup of hypomagnesemia-associated seizures.
Results:
Hypomagnesemia contributed to the cause of the seizures in all 3 cases. Various causes of hypomagnesemia were investigated, including genetic etiologies. All 3 patients were maintained at a magnesium level >0.65 mmol/L, which improved or eliminated the seizures.
Significance:
Magnesium levels should always be measured when trying to determine the etiology of seizures. Hypomagnesemia and afebrile seizures should be treated with the goal of maintaining a magnesium concentration >0.65 mmol/L. Although rare, genetic causes of hypomagnesemia should be considered, once common causes of hypomagnesemia are ruled out.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>28503619</pmid><doi>10.1177/2329048X16674834</doi><oa>free_for_read</oa></addata></record> |
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subjects | Original |
title | Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature |
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