We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a small Southern Italian town. The patient was pancytopenic when she was 31, and was found to be aplastic at the age of 34. Spontaneous chromosomal breakages were not evident in peripheral blood lymphocyte cultures but the diepoxybutane (DEB) test, carried out during the aplastic phase, was clearly positive. Danazol treatment significantly improved her hematological condition, yielding a Hb peak value of 13.4 g/dL. Four years later moderate pancytopenia has recurred. This case demonstrates that even adult pancytopenic patients may have FA and that a test detecting chromosomal hypersensitivity to cross-linking agents is the only key to a correc...
Fanconi anemia (FA) is a rare inherited syndrome with diverse clinical symptoms including developmen...
Diagnóstico citogenético e molecular da anemia de Fanconi hyper-pigmentation, kidney and urinary tra...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a...
Background: Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by short statur...
Fanconi Anemia (FA) is a rare autosomal recessive disorder affecting multiple body systems. The diag...
We describe a 56-year-old woman suspected of Fanconi anemia on the basis of the following clinical f...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi’s anemia (FA) alson called Fanconi Pancytopenia is a rare, potentially life-threatening fail...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Introduction: Fanconi anemia is an autosomal recessive disease characterized by congenital abnormali...
Background and objective: Fanconi anemia is a rare inherited autosomal recessive disease characteriz...
Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of synd...
Fanconi syndrome was first described in 1927 by G.Fanconi. Fanconi syndrome with congenital aplastic...
Fanconi anemia is the most common of the rare inherited bone marrow failure syndromes. It is caused ...
Fanconi anemia (FA) is a rare inherited syndrome with diverse clinical symptoms including developmen...
Diagnóstico citogenético e molecular da anemia de Fanconi hyper-pigmentation, kidney and urinary tra...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a...
Background: Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by short statur...
Fanconi Anemia (FA) is a rare autosomal recessive disorder affecting multiple body systems. The diag...
We describe a 56-year-old woman suspected of Fanconi anemia on the basis of the following clinical f...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi’s anemia (FA) alson called Fanconi Pancytopenia is a rare, potentially life-threatening fail...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Introduction: Fanconi anemia is an autosomal recessive disease characterized by congenital abnormali...
Background and objective: Fanconi anemia is a rare inherited autosomal recessive disease characteriz...
Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of synd...
Fanconi syndrome was first described in 1927 by G.Fanconi. Fanconi syndrome with congenital aplastic...
Fanconi anemia is the most common of the rare inherited bone marrow failure syndromes. It is caused ...
Fanconi anemia (FA) is a rare inherited syndrome with diverse clinical symptoms including developmen...
Diagnóstico citogenético e molecular da anemia de Fanconi hyper-pigmentation, kidney and urinary tra...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...