Add to ORKGBackground: Fanconi anemia (FA) is a chromosomal breakage disorder characterized by familial aplastic anemia (AA), various congenital anomalies, and a characteristic chromosomal response to clastogenic stress. Methods: In this study, chromosome breakage test was performed for 38 patients suspected of having FA and age-matched controls. Results: According to the results, ten patients were considered as FA cases and 15 patients with no chro-mosomal breaks were considered as AA. Conclusion: Differentiation of FA from AA is very important because the primary treatment is different. This test should be done in every primary presentation of AA
Introduction: Fanconi anemia is an autosomal recessive disease characterized by congenital abnormali...
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a...
Background: Fanconi anemia (FA) is an autosomal recessive, cancer susceptibility disorder characteri...
Background: Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by short statur...
Background and Objective: Fanconi anemia is the most prevalent inherited aplastic anemia. Diagnosis ...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of synd...
Fanconi anemia (FA) is a rare inherited syndrome with diverse clinical symptoms including developmen...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Background: Fanconi anemia (FA) is a rare autosomal recessive genetic disorder that shows an increas...
Fanconi Anemia (FA) is a rare autosomal recessive disorder affecting multiple body systems. The diag...
Background and objective: Fanconi anemia is a rare inherited autosomal recessive disease characteriz...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia (FA) is a rare form of an inherited disorder that mainly results in aplastic anemia. ...
Fanconi anemia (FA) is a recessively inherited disease characterized by multiple symptoms including ...
Introduction: Fanconi anemia is an autosomal recessive disease characterized by congenital abnormali...
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a...
Background: Fanconi anemia (FA) is an autosomal recessive, cancer susceptibility disorder characteri...
Background: Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by short statur...
Background and Objective: Fanconi anemia is the most prevalent inherited aplastic anemia. Diagnosis ...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of synd...
Fanconi anemia (FA) is a rare inherited syndrome with diverse clinical symptoms including developmen...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Background: Fanconi anemia (FA) is a rare autosomal recessive genetic disorder that shows an increas...
Fanconi Anemia (FA) is a rare autosomal recessive disorder affecting multiple body systems. The diag...
Background and objective: Fanconi anemia is a rare inherited autosomal recessive disease characteriz...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia (FA) is a rare form of an inherited disorder that mainly results in aplastic anemia. ...
Fanconi anemia (FA) is a recessively inherited disease characterized by multiple symptoms including ...
Introduction: Fanconi anemia is an autosomal recessive disease characterized by congenital abnormali...
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a...
Background: Fanconi anemia (FA) is an autosomal recessive, cancer susceptibility disorder characteri...