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Epilepsy and Electrophysiological Findings in Polish Twins With Glycogenosis Type IIIb
Glycogen storage diseases are rare genetic disorders, mostly autosomal recessively inherited. Abnormal accumulation is because of the lack of one of the enzymes involved in glycogen metabolism. Neurological manifestation of the diseases involves muscle weakness and hypoglycemia-induced seizures. In...
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Published in: | Clinical EEG and neuroscience 2014-07, Vol.45 (3), p.201-204 |
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description | Glycogen storage diseases are rare genetic disorders, mostly autosomal recessively inherited. Abnormal accumulation is because of the lack of one of the enzymes involved in glycogen metabolism. Neurological manifestation of the diseases involves muscle weakness and hypoglycemia-induced seizures. In this article, we present a history of twin sisters with unusual coincidence of glycogenosis type IIIb and epilepsy. Hypoglycemic background of seizures and organic changes of the central nervous system were excluded. Since the introduction of antiepileptic treatment, the patients have been seizure-free; however, paroxysmal electroencephalographic (EEG) changes have persisted. A high-protein and low-carbohydrate diet has protected them against hypoglycemia. |
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A high-protein and low-carbohydrate diet has protected them against hypoglycemia.</description><identifier>ISSN: 1550-0594</identifier><identifier>EISSN: 2169-5202</identifier><identifier>DOI: 10.1177/1550059413500276</identifier><identifier>PMID: 24357677</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Age ; Anticonvulsants - therapeutic use ; Brain damage ; Brain Mapping - methods ; Brain research ; Cerebral Cortex - drug effects ; Cerebral Cortex - physiopathology ; Child, Preschool ; Combined Modality Therapy ; Consciousness ; Diabetes ; Diet, Carbohydrate-Restricted ; Dietary Proteins - administration & dosage ; Disease ; Diseases in Twins - diagnosis ; Diseases in Twins - genetics ; Diseases in Twins - physiopathology ; Diseases in Twins - therapy ; Electroencephalography - methods ; Enzymes ; Epilepsy - diagnosis ; Epilepsy - genetics ; Epilepsy - physiopathology ; Epilepsy - therapy ; Female ; Follow-Up Studies ; Genetic Carrier Screening ; Glucose ; Glycogen Storage Disease Type III - diagnosis ; Glycogen Storage Disease Type III - genetics ; Glycogen Storage Disease Type III - physiopathology ; Humans ; Hypoglycemia ; Infant ; Infant, Newborn ; Neurology ; NMR ; Nuclear magnetic resonance ; Pediatrics ; Poland ; Signal Processing, Computer-Assisted ; Spasms, Infantile - diagnosis ; Spasms, Infantile - genetics ; Spasms, Infantile - physiopathology ; Spasms, Infantile - therapy</subject><ispartof>Clinical EEG and neuroscience, 2014-07, Vol.45 (3), p.201-204</ispartof><rights>EEG and Clinical Neuroscience Society (ECNS) 2013</rights><rights>Copyright SAGE PUBLICATIONS, INC. 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-287dede1893fb9b7f8376b9e92311c7ec130479d52b45d26f295a175e3e029ca3</citedby><cites>FETCH-LOGICAL-c332t-287dede1893fb9b7f8376b9e92311c7ec130479d52b45d26f295a175e3e029ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906,79113</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24357677$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kroczka, Sławomir</creatorcontrib><creatorcontrib>Biedroń, Agnieszka</creatorcontrib><creatorcontrib>Kaciński, Marek</creatorcontrib><title>Epilepsy and Electrophysiological Findings in Polish Twins With Glycogenosis Type IIIb</title><title>Clinical EEG and neuroscience</title><addtitle>Clin EEG Neurosci</addtitle><description>Glycogen storage diseases are rare genetic disorders, mostly autosomal recessively inherited. Abnormal accumulation is because of the lack of one of the enzymes involved in glycogen metabolism. Neurological manifestation of the diseases involves muscle weakness and hypoglycemia-induced seizures. In this article, we present a history of twin sisters with unusual coincidence of glycogenosis type IIIb and epilepsy. Hypoglycemic background of seizures and organic changes of the central nervous system were excluded. Since the introduction of antiepileptic treatment, the patients have been seizure-free; however, paroxysmal electroencephalographic (EEG) changes have persisted. A high-protein and low-carbohydrate diet has protected them against hypoglycemia.</description><subject>Age</subject><subject>Anticonvulsants - therapeutic use</subject><subject>Brain damage</subject><subject>Brain Mapping - methods</subject><subject>Brain research</subject><subject>Cerebral Cortex - drug effects</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Child, Preschool</subject><subject>Combined Modality Therapy</subject><subject>Consciousness</subject><subject>Diabetes</subject><subject>Diet, Carbohydrate-Restricted</subject><subject>Dietary Proteins - administration & dosage</subject><subject>Disease</subject><subject>Diseases in Twins - diagnosis</subject><subject>Diseases in Twins - genetics</subject><subject>Diseases in Twins - physiopathology</subject><subject>Diseases in Twins - therapy</subject><subject>Electroencephalography - methods</subject><subject>Enzymes</subject><subject>Epilepsy - diagnosis</subject><subject>Epilepsy - genetics</subject><subject>Epilepsy - physiopathology</subject><subject>Epilepsy - therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Genetic Carrier Screening</subject><subject>Glucose</subject><subject>Glycogen Storage Disease Type III - diagnosis</subject><subject>Glycogen Storage Disease Type III - genetics</subject><subject>Glycogen Storage Disease Type III - physiopathology</subject><subject>Humans</subject><subject>Hypoglycemia</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Neurology</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pediatrics</subject><subject>Poland</subject><subject>Signal Processing, Computer-Assisted</subject><subject>Spasms, Infantile - diagnosis</subject><subject>Spasms, Infantile - genetics</subject><subject>Spasms, Infantile - physiopathology</subject><subject>Spasms, Infantile - therapy</subject><issn>1550-0594</issn><issn>2169-5202</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kM9LwzAcxYMobk7vniTguZofTdMcZWyzMNDD1GNJ02-7jK6pTcfof2_Hpojg6R3e570HD6FbSh4olfKRCkGIUCHlgzIZnaExo5EKBCPsHI0PdnDwR-jK-w0hPGI8vEQjFnIhIynH6H3W2Aoa32Nd53hWgela16x7b13lSmt0hee2zm1demxr_Ooq69d4tbe1xx-2W-NF1RtXQu289XjVN4CTJMmu0UWhKw83J52gt_lsNX0Oli-LZPq0DAznrAtYLHPIgcaKF5nKZBFzGWUKFOOUGgmGchJKlQuWhSJnUcGU0FQK4ECYMppP0P2xt2nd5w58l27crq2HyZSKcHiBKhYPFDlSpnXet1CkTWu3uu1TStLDkenfI4fI3al4l20h_wl8PzcAwRHwuoRfq_8VfgE2x3mN</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Kroczka, Sławomir</creator><creator>Biedroń, Agnieszka</creator><creator>Kaciński, Marek</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20140701</creationdate><title>Epilepsy and Electrophysiological Findings in Polish Twins With Glycogenosis Type IIIb</title><author>Kroczka, Sławomir ; 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Abnormal accumulation is because of the lack of one of the enzymes involved in glycogen metabolism. Neurological manifestation of the diseases involves muscle weakness and hypoglycemia-induced seizures. In this article, we present a history of twin sisters with unusual coincidence of glycogenosis type IIIb and epilepsy. Hypoglycemic background of seizures and organic changes of the central nervous system were excluded. Since the introduction of antiepileptic treatment, the patients have been seizure-free; however, paroxysmal electroencephalographic (EEG) changes have persisted. A high-protein and low-carbohydrate diet has protected them against hypoglycemia.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>24357677</pmid><doi>10.1177/1550059413500276</doi><tpages>4</tpages></addata></record> |
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subjects | Age Anticonvulsants - therapeutic use Brain damage Brain Mapping - methods Brain research Cerebral Cortex - drug effects Cerebral Cortex - physiopathology Child, Preschool Combined Modality Therapy Consciousness Diabetes Diet, Carbohydrate-Restricted Dietary Proteins - administration & dosage Disease Diseases in Twins - diagnosis Diseases in Twins - genetics Diseases in Twins - physiopathology Diseases in Twins - therapy Electroencephalography - methods Enzymes Epilepsy - diagnosis Epilepsy - genetics Epilepsy - physiopathology Epilepsy - therapy Female Follow-Up Studies Genetic Carrier Screening Glucose Glycogen Storage Disease Type III - diagnosis Glycogen Storage Disease Type III - genetics Glycogen Storage Disease Type III - physiopathology Humans Hypoglycemia Infant Infant, Newborn Neurology NMR Nuclear magnetic resonance Pediatrics Poland Signal Processing, Computer-Assisted Spasms, Infantile - diagnosis Spasms, Infantile - genetics Spasms, Infantile - physiopathology Spasms, Infantile - therapy |
title | Epilepsy and Electrophysiological Findings in Polish Twins With Glycogenosis Type IIIb |
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