View Fanconi Anemia Bone Marrow Images
View Fanconi Anemia Bone Marrow Images. It is passed from parents to children. In 1927, guido fanconi first reported 3 brothers with macrocytosis, pancytopenia, and physical abnormalities.
A genetic test is necessary to establish a diagnosis of fa.
Fanconi anemia (fa) is an autosomal recessive inherited condition in which congenital malformations are associated with bone marrow failure. Fanconi anemia is the most common bone marrow failure syndrome. The most common abnormalities are skin pigmentation, microcephaly, short stature. Fanconi's anemia (fa) is an autosomal recessive inherited condition in which congenital malformations are associated with bone marrow failure.
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