24 top medical experts on Type I Schindler Disease across 5 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type I Schindler Disease: A rare clinically heterogeneous type of NAGA deficiency with developmental, neurologic and psychiatric manifestations presenting at an intermediate age.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Alpha-Galactosidase B Deficiency,  Schindler Type Alpha-Galnac Deficiency,  Alpha-N-Acetylgalactosaminidase Deficiency,  Adult-Onset Alpha-N-Acetylgalactosaminidase Deficiency,  Type I Alpha-N-Acetylgalactosaminidase Deficiency,  Type III Alpha-N-Acetylgalactosaminidase Deficiency,  Alpha-N-acetylgalactosaminidase deficiency adult onset,  Alpha-N-acetylgalactosaminidase deficiency type 2,  type 1 Alpha-N-acetylgalactosaminidase deficiency,  Alpha-Naga Deficiency,  Angiokeratoma Corporis Diffusum-Glycopeptiduria,  Galb Deficiency,  Kanzaki disease,  Lysosomal Glycoaminoacid Storage Disease-Angiokeratoma Corporis Diffusum,  Type II NAGA Deficiency,  Type III NAGA Deficiency,  NAGA deficiency type 2,  Naga Deficiency,  Type I Naga Deficiency,  Schindler type Neuroaxonal dystrophy,  Schindler Type Neuronal Axonal Dystrophy,  Schindler Disease,  Type II Schindler Disease,  Type III Schindler Disease,  type 1 Schindler disease,  type 2 Schindler disease,  Type II alpha-N-Acetylgalactosaminidase Deficiency


  

        

                    


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