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Genetic Forms of Iron Deficiency Anaemia


Clinical observations of unexplained forms of iron deficiency anaemia, coupled with growing evidence of inherited disorders and advances in knowledge concerning iron metabolism, have led to the description of five new genetic forms of iron deficiency anaemia. In this webcase, Dr. Photis Beris discusses these rare but important diseases and how to distinguish them from other forms of microcytic anaemia.
Faculty
Photis Beris, MD
Photis Beris, MD
Professor of Haematology
Chairman of the Department
  of Haematology
National and Kapodistrian University
  of Athens School of Medicine
Laiko University Hospital
Athens, Greece

Target Audience

This activity is designed for haematologists, medical oncologists, haematology-oncology specialists, and other healthcare professionals involved in the screening, evaluation, treatment, and management of patients with genetic forms of iron deficiency anaemia.

Learning Objectives


After participating in this activity, participants should be better able to:
  • Based on knowledge of their biologic and clinical features, differentiate between DMT1 mutation-related anaemia, glutaredoxin 5 mutation-related anaemia, hypotransferrinaemia/atransferrinaemia, aceruloplasminaemia, and iron refractory iron deficiency anaemia (IRIDA) in order to accurately identify and diagnose patients with these disorders.
  • Based on the genetic mutations involved, apply your knowledge of the mechanisms of action of DMT1 mutation-related anaemia, glutaredoxin 5 mutation-related anaemia, hypotransferrinaemia/ atransferrinaemia, aceruloplasminaemia, and iron refractory iron deficiency anaemia (IRIDA) in order to better understand the pathology of these diseases.
Disclosure Information

Photis Beris, MD, Photis Beris, MD, has received grant/research support from, is on the speakers bureau of, and is on the advisory board for Novartis Pharmaceuticals Corporation; and is a consultant for Vifor International.

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