214 top medical experts on Glycosylphosphatidylinositol deficiency across 26 countries and 10 U.S. states, including 25 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Glycosylphosphatidylinositol deficiency: A rare congenital disorder of glycosylation characterized by cerebral and portal vein thrombosis, portal hypertension, macrocephaly, and persistent absence seizures. Additional reported features include mild to moderate global developmental delay and intellectual disability, as well as thrombocytopenia. Brain imaging may show variable stages of infarction and cerebral and cerebellar atrophy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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