Fanconi Anemia – Rare Cause of Pancytopenia at Child

Authors

  • D. Voda Transilvania University of Brasov, Romania
  • A. Deaconu Children Hospital of Brasov, Romania
  • A.S. Musat Children Hospital of Brasov, Romania

Keywords:

Fanconi Anemia, pancytopenia, thrombocytopenia, FANC genes, bone-marrow failure

Abstract

In this article, we present two cases of children (sister and brother) who present Fanconi anemia. Fanconi aplastic anemia was discovered in 1927. In 99% of the cases, it is transmitted autosomal recessive. The ratio between the sexes is about equal. It is usually diagnosed in children between 5-15 years. A positive diagnosis is based on the following criteria: 1. clinical (morphological abnormalities, anemic syndrome, infection, bleeding), 2. hematologic (pancytopenia, macrocytic anemia, and marrow failure), 3. chromosome fragility.

Author Biography

D. Voda, Transilvania University of Brasov, Romania

Faculty of Medicine

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Published

2012-09-18

Issue

Section

MEDICAL SCIENCES