205 top medical experts on Griscelli syndrome type 2 across 25 countries and 7 U.S. states, including 34 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Griscelli syndrome type 2: A rare subtype of Griscelli syndrome characterized by pigmentary dilution in skin and hair with irregular clumps of pigment in hair shafts resulting in silvery hair, in association with increased susceptibility to recurrent infections and immunological abnormalities, in particular impairment of T-cell and natural killer cytotoxic activity eventually leading to hemophagocytic lymphohistiocytosis. Patients may present neurological manifestations related to infiltration of the central nervous system in the context of the hemophagocytic syndrome. The disease is mostly fatal in the first decade of life.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
    • Jeffrey Modell Foundation (JMF)
      780 Third Ave
      New York, NY 10017
      Fax: 212-764-4180
      E-mail: info@jmfworld.org
      Website: http://www.info4pi.org/
      JMF is a global patient organization devoted to early and precise diagnosis, meaningful treatments, and ultimately, cures - through clinical and basic research, physician education, patient support, advocacy, public awareness and newborn screening.

Organizations Providing General Support

  • Synonyms: partial with immunodeficiency Albinism,  Type 2 Griscelli Syndrome,  Griscelli syndrome with hemophagocytic syndrome,  Partial Albinism And Immunodeficiency Syndrome,  Partial albinism and immunodeficiency


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