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Coinheritance of Gaucher disease and ?-thalassemia resulting in confusion between two inherited hematologic diseases.

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 ?-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.

SUBMITTER: Miri-Moghaddam E

PROVIDER: S-EPMC3352325 | biostudies-literature | 2011 Jan

REPOSITORIES: biostudies-literature

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Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases.

Miri-Moghaddam Ebrahim E Velayati Arash A Naderi Majid M Tayebi Nahid N Sidransky Ellen E

Blood cells, molecules & diseases 20100916 1

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 ...[more]

PMID: 20846888

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