202 top medical experts on Pelger-Huet Anomaly across 20 countries and 15 U.S. states, including 18 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Pelger-Huet Anomaly: Autosomal dominant anomaly characterized by abnormal ovoid shape granulocyte nuclei and their clumping chromatin. Mutations in the lamin B receptor gene that results in reduced protein levels are associated with the disorder. Heterozygote individuals are healthy with normal granulocyte function while homozygote individuals occasionally have skeletal anomalies, developmental delay, and seizures.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Genetic Diseases (2,477), Leukocyte Disorders (759).


  

        

                    


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