Movement Disorders
|
0.200 |
Biomarker
|
group |
HPO |
|
|
|
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay.
|
1714544 |
1991 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.
|
10766892 |
2000 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Seizure characterization and electroencephalographic features in Glut-1 deficiency syndrome.
|
12752470 |
2003 |
Movement Disorders
|
0.200 |
Biomarker
|
group |
BEFREE |
This case broadens the phenotype of GLUT1 deficiency and illustrates the importance of cerebrospinal fluid (CSF) evaluation in detecting potentially treatable conditions in children with undiagnosed movement disorders.
|
16149086 |
2006 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
|
18577546 |
2008 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.
|
19798636 |
2009 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Autosomal recessive inheritance of GLUT1 deficiency syndrome.
|
20221955 |
2009 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
|
20129935 |
2010 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Glut1 deficiency: inheritance pattern determined by haploinsufficiency.
|
20687207 |
2010 |
Movement Disorders
|
0.200 |
Biomarker
|
group |
BEFREE |
Gait disturbances and movement disorders are frequent in patients with Glut-1 deficiency and are signs of chronic and intermittent pyramidal, cerebellar and extrapyramidal circuit dysfunction.
|
20063428 |
2010 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome.
|
21791420 |
2011 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.
|
21555602 |
2011 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.
|
21832227 |
2011 |
Movement Disorders
|
0.200 |
Biomarker
|
group |
BEFREE |
GLUT1-DS is characterized by movement disorders, including paroxysmal exercise-induced dystonia (PED), as well as seizures, mental retardation and hypoglycorrhachia.
|
21229316 |
2011 |
Movement Disorders
|
0.200 |
GeneticVariation
|
group |
BEFREE |
A part from this classic phenotype, clinical conditions associated with a deficiency of GLUT1 are highly variable and several atypical variants have been described; in particular, patients with movement disorders, but without seizures, with paroxysmal exertion-induced dyskinesia, have been reported.
|
21962875 |
2012 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutation.
|
22492876 |
2012 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
|
23280796 |
2012 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Unusual sensitivity to steroid treatment in intractable childhood epilepsy suggests GLUT1 deficiency syndrome.
|
22976442 |
2012 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
The role of SLC2A1 in early onset and childhood absence epilepsies.
|
23306390 |
2013 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS).
|
23443458 |
2013 |
Movement Disorders
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Familial paroxysmal exercise-induced dyskinesia (PED) is a rare movement disorder that is mostly caused by mutations in the solute carrier family 2, member 1 (SLC2A1) gene and inherited in an autosomal dominant manner.
|
25099510 |
2014 |
Movement Disorders
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.
|
24963779 |
2014 |
Movement Disorders
|
0.200 |
Biomarker
|
group |
BEFREE |
No significant differences were found in terms of type of movement disorder, whilst Paroxysmal Exertion-induced Dyskinesia (PED) is confirmed to be the most characteristic movement disorder type in GLUT1DS.
|
25564316 |
2015 |
Movement Disorders
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Mutations in SLC2A1 were detected in 5 (10%) of 50 patients with absence epilepsy, and in one (2.7%) of 37 patient with unselected epilepsies, ID, and/or various movement disorders.
|
26537434 |
2015 |