Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2827882 | Blood Cells, Molecules, and Diseases | 2011 | 4 Pages |
Abstract
Gaucher type 1 disease has a wide spectrum of phenotypes ranging from asymptomatic individuals to patients with massive hepatosplenomegaly and bone involvement. In most, anemia, thrombocytopenia and splenomegaly are the primary manifestations at diagnosis, findings shared by the hemoglobinopathies. Here we report the co-inheritance of α-thalassemia and Gaucher disease in a consanguineous family followed in Iran, which resulted in confusion regarding the diagnosis. This report emphasizes the need to independently establish the diagnosis of every affected member of a family to ensure appropriate management and therapeutic decisions.
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Authors
Ebrahim Miri-Moghaddam, Arash Velayati, Majid Naderi, Nahid Tayebi, Ellen Sidransky,