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Disease: Navajo poikiloderma

  • Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients
  • Clericuzio-type Poikiloderma with Neutropenia Syndrome in a Turkish Family: a Three Report of Siblings with Mutation in the C16orf57 gene
  • Hyperbaric oxygen management of recurrent cellulitis in poikiloderma with neutropenia
  • Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia
  • Poikiloderma with Neutropenia in Morocco: a Report of Four Cases
  • Poikiloderma with neutropenia, Clericuzio type, in a family from Morocco
  • Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria
  • Poikiloderma with neutropenia: report of three cases including one with calcinosis cutis
  • Southwestern Athabaskan (Navajo and Apache) genetic diseases
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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