Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Exercise and fasting induced movement disorder in children: think of the GLUT1 deficiency syndrome].

Nederlands tijdschrift voor geneeskunde - 13 Jul 2018

van Kan Kim E M, Panis Bianca

Abstract excerpt

BACKGROUND: Glucose transporter type 1 (GLUT1) enables glucose to pass through the blood-brain barrier. A hereditary deficiency of this protein may lead to clinical symptoms when blood glucose levels are decreasing. CASE DESCRIPTION: A 7-year-old girl with therapy-resistant childhood absence epilepsy presented with an exercise and fasting induced dystonic and atactic movement pattern. The movement pattern...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Carbohydrate Metabolism, Inborn Errors
Share to Diet, Ketogenic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Epilepsy, Absence

Share to Exercise

Share to Fasting

Share to Glucose Transporter Type 1

Share to Monosaccharide Transport Proteins

Share to Movement Disorders

Source

Identifiers

PMID: 30040286

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Exercise and fasting induced movement disorder in children: think of the GLUT1 deficiency syndrome].PMID 30040286Read ↗

The glucose transporter type 1 (Glut1) syndromes.Semantic proximity Read ↗

[Glucose transporter protein type 1 (GLUT-1) deficiency syndrome].Semantic proximity Read ↗

GLUT1 deficiency syndrome: an update.Semantic proximity Read ↗

Phenotypic variability of GLUT1 deficiency: When is necessary to suspect?Semantic proximity Read ↗

Diagnosis and treatment recommendations for glucose transporter 1 deficiency syndromeSemantic proximity Read ↗

[GLUT-1 deficiency syndrome or De Vivo disease: a case report].Semantic proximity Read ↗

Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?Semantic proximity Read ↗

Glucose transporter type 1 deficiency syndrome: clinical aspects, diagnosis, and treatment.Semantic proximity Read ↗

Atypical Manifestations in Glut1 Deficiency Syndrome.Semantic proximity Read ↗

Glut1 deficiency: when to suspect and how to diagnose?Semantic proximity Read ↗

Refractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review.Semantic proximity Read ↗

Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic dietSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.