22 top medical experts on Hemolytic Anemia due to Uridine 5-Prime Monophosphate Hydrolase Deficiency across 4 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hemolytic Anemia due to Uridine 5-Prime Monophosphate Hydrolase Deficiency: Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency is a rare, hereditary, hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by mild to moderate hemolytic anemia associated with basophilic stippling and the accumulation of high concentrations of pyrimidine nucleotides within the erythrocyte. Patients present with variable features of jaundice, splenomegaly, hepatomegaly, gallstones, and sometimes require transfusions. Rare cases of mild development delay and learning difficulties are reported.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Hemolytic Anemia due to P5N Deficiency,  Hemolytic Anemia due to UMPH1 Deficiency,  Hemolytic Anemia due to Pyrimidine 5-Prime Nucleotidase Deficiency,  UMPH1 Deficiency


  

        

                    


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