Disease #00544 (GLUT1DS1 (GLUT1 deficiency syndrome, type 1, infantile onset, severe (GLUT1DS-1)), OMIM:606777)

Official abbreviation GLUT1DS1
Name GLUT1 deficiency syndrome, type 1, infantile onset, severe (GLUT1DS-1)
OMIM ID 606777
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 9
Phenotype entries for this disease 9
Associated with 1 gene SLC2A1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

9 entries on 1 page. Showing entries 1 - 9.
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00037116 - - - - - Germany - - - - - GLUT1DS1 GLUT1-deficiency SLC2A1 SLC2A1 1 1 Andreas Laner
00037118 - - - - - Germany - - - - - GLUT1DS1 GLUT1-deficiency SLC2A1 SLC2A1 1 1 Andreas Laner
00037119 - - - - - Germany - - - - - GLUT1DS1 GLUT1-deficiency: epilepsy (Absences, atonisch), ataxia, global developmental retardation, dystonia SLC2A1 SLC2A1 1 1 Andreas Laner
00037129 - - - - - Germany - - - - - GLUT1DS1 GLUT1-deficiency syndrome, difficult epilepsy, Borderline, low CSF glucose SLC2A1 SLC2A1 1 1 Andreas Laner
00080889 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - GLUT1DS1 GLUT1 deficiency syndrome 1 (OMIM:606777) SLC2A1 SLC2A1 1 1 Daniel Trujillano
00081421 - - - F - Netherlands white - - - - GLUT1DS1 5m myoclonic seizures; severe intellectual disability (IQ ~50); “clumsy” in the mornings, with clear improvement after breakfast, but never noticed episodes that might fit with a diagnosis of paroxysmal dyskinesia SLC2A1 SLC2A1 1 1 Erik-Jan Kamsteeg
00100280 - - - - - Germany - - - - - GLUT1DS1 - SLC2A1 SLC2A1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00377142 177772 - - F no Germany - - - - - GLUT1DS1 clinically suspicion of GLUT1 deficiency syndrome KCNQ3 KCNQ3 1 1 Andreas Laner
00415082 202584 - - M - Germany - - - - - GLUT1DS1 Episodic ataxia SLC2A1 SLC2A1 1 1 Andreas Laner
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