225 top medical experts on Glut1 Deficiency Syndrome across 34 countries and 17 U.S. states, including 47 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Glut1 Deficiency Syndrome: Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Social Networking Websites

  • RareConnect has an online community for patients and families with this condition so they can connect with others and share their experiences living with a rare disease. The project is a joint collaboration between EURORDIS (European Rare Disease Organisation) and NORD (National Organization for Rare Disorders).
  • Synonyms: De Vivo disease,  Encephalopathy Due To Glut1 Deficiency,  GLUT-1 deficiency syndrome,  Glucose Transporter Protein Syndrome,  Glucose Transporter Type 1 Deficiency Syndrome,  blood-brain barrier Glucose transport defect,  Glucose transporter type1 (GLUT-1) deficiency


    •   

            

                        


      Computing Expert Listing ...