GLUT1 deficiency syndrome, also known as GLUT1-DS, De Vivo disease or Glucose transporter type 1 deficiency syndrome, is an autosomal dominant genetic...

and II. GLUT1 accounts for 2 percent of the protein in the plasma membrane of erythrocytes. Mutations in this gene can cause GLUT1 deficiency syndrome...

can only manage toe walking. Toe walking is a symptom in those with GLUT1 deficiency Syndrome. There are many health professionals who assess and treat...

cause abnormal electrochemical discharges that result in seizures GLUT1 deficiency syndrome Anorexia nervosa, bulimia nervosa, and other eating disorders...

movements, termed aberrant gaze saccades, are an early symptom of GLUT1 deficiency syndrome in infancy.[non-primary source needed] When the brain is led...

syndrome GLUT1 deficiency syndrome Griscelli syndrome Type 1 (Elejalde syndrome) Holocarboxylase synthetase deficiency / Multiple carboxylase deficiency Krabbe...

discovery of mutations in uniporters has been linked to diseases such as GLUT1 deficiency syndrome, cystic fibrosis, Hartnup disease, primary hyperoxaluria and...

diseases and agents. It is a symptom of several diseases, including GLUT1 deficiency syndrome, Lesch–Nyhan syndrome, phenylketonuria, and Huntington disease...

include genetic disorders such as Down syndrome, Fragile X syndrome and GLUT1 Deficiency Syndrome; childhood infections such as meningitis or encephalitis,...

breast, lung, or ovarian cancer in adults. Other considerations include GLUT1 Deficiency Syndrome, multiple sclerosis, toxins, medication effects (e.g. Serotonin...