Glucose Transporter Type 1 Deficiency Syndrome with Carbohydrate-Responsive Symptoms but without Epilepsy
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| Title: | Glucose Transporter Type 1 Deficiency Syndrome with Carbohydrate-Responsive Symptoms but without Epilepsy |
|---|---|
| Language: | English |
| Authors: | Koy, Anne, Assmann, Birgit, Klepper, Joerg, Mayatepek, Ertan |
| Source: | Developmental Medicine & Child Neurology. Dec 2011 53(12):1154-1156. |
| Availability: | Wiley-Blackwell. 350 Main Street, Malden, MA 02148. Tel: 800-835-6770; Tel: 781-388-8598; Fax: 781-388-8232; e-mail: cs-journals@wiley.com; Web site: http://www.wiley.com/WileyCDA/ |
| Peer Reviewed: | Y |
| Page Count: | 3 |
| Publication Date: | 2011 |
| Document Type: | Journal Articles Reports - Research |
| Descriptors: | Intelligence, Epilepsy, Dietetics, Developmental Delays, Motor Development, Cognitive Development, Metabolism, Physical Disabilities, Human Body, Females, Young Children, Psychomotor Skills, Child Development, Genetics, Visual Perception, Spatial Ability, Speech Skills |
| DOI: | 10.1111/j.1469-8749.2011.04082.x |
| ISSN: | 0012-1622 |
| Abstract: | Glucose transporter type 1 deficiency syndrome (GLUT1-DS) is caused by a defect in glucose transport across the blood-brain barrier. The main symptoms are epilepsy, developmental delay, movement disorders, and deceleration of head circumference. A ketogenic diet has been shown to be effective in controlling epilepsy in GLUT1-DS. We report a female child (3y 4mo) who presented with delayed psychomotor development and frequent episodes of staggering, impaired vigilance, and vomiting that resolved promptly after food intake. Electroencephalography was normal. The cerebrospinal fluid-blood glucose ratio was 0.42 (normal greater than or equal to 0.45). GLUT1-DS was confirmed by molecular genetic testing, which showed a novel "de novo" heterozygous mutation in the "SLC2A1" gene (c.497_499delTCG, "p."VAL166del). Before starting a ketogenic diet, the child's cognitive development was tested using the Snijders-Oomen Non-Verbal Intelligence Test, which revealed a heterogeneous intelligence profile with deficits in her visuomotor skills and spatial awareness. Her motor development was delayed. Three months after introducing a ketogenic diet, she showed marked improvement in speech and motor development, as tested by the Movement Assessment Battery for Children (manual dexterity 16th centile, ball skills 1st centile, static and dynamic balance 5th centile). This case demonstrates that GLUT1-DS should be investigated in individuals with unexplained developmental delay. Epilepsy is not a mandatory symptom. The ketogenic diet is also beneficial for non-epileptic symptoms in GLUT1-DS. |
| Abstractor: | As Provided |
| Entry Date: | 2012 |
| Accession Number: | EJ948869 |
| Database: | ERIC |
| FullText | Links: – Type: pdflink Url: https://content.ebscohost.com/cds/retrieve?content=AQICAHj0k_4E0hTGH8RJwT4gCJyBsGNe_WN95AvKlDbXJGqwxwEXDTFaMO1Ew6bWYRNk7b2GAAAA4jCB3wYJKoZIhvcNAQcGoIHRMIHOAgEAMIHIBgkqhkiG9w0BBwEwHgYJYIZIAWUDBAEuMBEEDKOnkqwXt3iMNAQkHgIBEICBmnvyl6-JZYBxugZsdtBqFEf_vi_D-qcn0KESTuX-NenBLTUd4Jr7FipAAfNyD8sHxe8dv_kB_Gv8s4NILvhIjvDo07GxYOuNMyWJtF4eohv5HAx1a4D17vWBLU8G1UAj4aPhOT4rv_CoWMHPdWEPg3qS5Y7qtF5AibxXNLzYxi5D4h-OoGndGa3iMFbeoJqsf9Pl56EZPD_VOEU= Text: Availability: 0 |
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| Header | DbId: eric DbLabel: ERIC An: EJ948869 AccessLevel: 3 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Glucose Transporter Type 1 Deficiency Syndrome with Carbohydrate-Responsive Symptoms but without Epilepsy – Name: Language Label: Language Group: Lang Data: English – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Koy%2C+Anne%22">Koy, Anne</searchLink><br /><searchLink fieldCode="AR" term="%22Assmann%2C+Birgit%22">Assmann, Birgit</searchLink><br /><searchLink fieldCode="AR" term="%22Klepper%2C+Joerg%22">Klepper, Joerg</searchLink><br /><searchLink fieldCode="AR" term="%22Mayatepek%2C+Ertan%22">Mayatepek, Ertan</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="SO" term="%22Developmental+Medicine+%26+Child+Neurology%22"><i>Developmental Medicine & Child Neurology</i></searchLink>. Dec 2011 53(12):1154-1156. – Name: Avail Label: Availability Group: Avail Data: Wiley-Blackwell. 350 Main Street, Malden, MA 02148. Tel: 800-835-6770; Tel: 781-388-8598; Fax: 781-388-8232; e-mail: cs-journals@wiley.com; Web site: http://www.wiley.com/WileyCDA/ – Name: PeerReviewed Label: Peer Reviewed Group: SrcInfo Data: Y – Name: Pages Label: Page Count Group: Src Data: 3 – Name: DatePubCY Label: Publication Date Group: Date Data: 2011 – Name: TypeDocument Label: Document Type Group: TypDoc Data: Journal Articles<br />Reports - Research – Name: Subject Label: Descriptors Group: Su Data: <searchLink fieldCode="DE" term="%22Intelligence%22">Intelligence</searchLink><br /><searchLink fieldCode="DE" term="%22Epilepsy%22">Epilepsy</searchLink><br /><searchLink fieldCode="DE" term="%22Dietetics%22">Dietetics</searchLink><br /><searchLink fieldCode="DE" term="%22Developmental+Delays%22">Developmental Delays</searchLink><br /><searchLink fieldCode="DE" term="%22Motor+Development%22">Motor Development</searchLink><br /><searchLink fieldCode="DE" term="%22Cognitive+Development%22">Cognitive Development</searchLink><br /><searchLink fieldCode="DE" term="%22Metabolism%22">Metabolism</searchLink><br /><searchLink fieldCode="DE" term="%22Physical+Disabilities%22">Physical Disabilities</searchLink><br /><searchLink fieldCode="DE" term="%22Human+Body%22">Human Body</searchLink><br /><searchLink fieldCode="DE" term="%22Females%22">Females</searchLink><br /><searchLink fieldCode="DE" term="%22Young+Children%22">Young Children</searchLink><br /><searchLink fieldCode="DE" term="%22Psychomotor+Skills%22">Psychomotor Skills</searchLink><br /><searchLink fieldCode="DE" term="%22Child+Development%22">Child Development</searchLink><br /><searchLink fieldCode="DE" term="%22Genetics%22">Genetics</searchLink><br /><searchLink fieldCode="DE" term="%22Visual+Perception%22">Visual Perception</searchLink><br /><searchLink fieldCode="DE" term="%22Spatial+Ability%22">Spatial Ability</searchLink><br /><searchLink fieldCode="DE" term="%22Speech+Skills%22">Speech Skills</searchLink> – Name: DOI Label: DOI Group: ID Data: 10.1111/j.1469-8749.2011.04082.x – Name: ISSN Label: ISSN Group: ISSN Data: 0012-1622 – Name: Abstract Label: Abstract Group: Ab Data: Glucose transporter type 1 deficiency syndrome (GLUT1-DS) is caused by a defect in glucose transport across the blood-brain barrier. The main symptoms are epilepsy, developmental delay, movement disorders, and deceleration of head circumference. A ketogenic diet has been shown to be effective in controlling epilepsy in GLUT1-DS. We report a female child (3y 4mo) who presented with delayed psychomotor development and frequent episodes of staggering, impaired vigilance, and vomiting that resolved promptly after food intake. Electroencephalography was normal. The cerebrospinal fluid-blood glucose ratio was 0.42 (normal greater than or equal to 0.45). GLUT1-DS was confirmed by molecular genetic testing, which showed a novel "de novo" heterozygous mutation in the "SLC2A1" gene (c.497_499delTCG, "p."VAL166del). Before starting a ketogenic diet, the child's cognitive development was tested using the Snijders-Oomen Non-Verbal Intelligence Test, which revealed a heterogeneous intelligence profile with deficits in her visuomotor skills and spatial awareness. Her motor development was delayed. Three months after introducing a ketogenic diet, she showed marked improvement in speech and motor development, as tested by the Movement Assessment Battery for Children (manual dexterity 16th centile, ball skills 1st centile, static and dynamic balance 5th centile). This case demonstrates that GLUT1-DS should be investigated in individuals with unexplained developmental delay. Epilepsy is not a mandatory symptom. The ketogenic diet is also beneficial for non-epileptic symptoms in GLUT1-DS. – Name: AbstractInfo Label: Abstractor Group: Ab Data: As Provided – Name: DateEntry Label: Entry Date Group: Date Data: 2012 – Name: AN Label: Accession Number Group: ID Data: EJ948869 |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/j.1469-8749.2011.04082.x Languages: – Text: English PhysicalDescription: Pagination: PageCount: 3 StartPage: 1154 Subjects: – SubjectFull: Intelligence Type: general – SubjectFull: Epilepsy Type: general – SubjectFull: Dietetics Type: general – SubjectFull: Developmental Delays Type: general – SubjectFull: Motor Development Type: general – SubjectFull: Cognitive Development Type: general – SubjectFull: Metabolism Type: general – SubjectFull: Physical Disabilities Type: general – SubjectFull: Human Body Type: general – SubjectFull: Females Type: general – SubjectFull: Young Children Type: general – SubjectFull: Psychomotor Skills Type: general – SubjectFull: Child Development Type: general – SubjectFull: Genetics Type: general – SubjectFull: Visual Perception Type: general – SubjectFull: Spatial Ability Type: general – SubjectFull: Speech Skills Type: general Titles: – TitleFull: Glucose Transporter Type 1 Deficiency Syndrome with Carbohydrate-Responsive Symptoms but without Epilepsy Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Koy, Anne – PersonEntity: Name: NameFull: Assmann, Birgit – PersonEntity: Name: NameFull: Klepper, Joerg – PersonEntity: Name: NameFull: Mayatepek, Ertan IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Type: published Y: 2011 Identifiers: – Type: issn-print Value: 0012-1622 Numbering: – Type: volume Value: 53 – Type: issue Value: 12 Titles: – TitleFull: Developmental Medicine & Child Neurology Type: main |
| ResultId | 1 |