Fanconi Anemia: What It Is, Symptoms, Causes & Treatment
2022年4月15日 · Fanconi anemia (FA) is a rare inherited condition that affects your bone marrow and many other parts of your body. Your bone marrow is the spongy tissue in the center of your bones that creates stem cells that become red and white blood cells and platelets.
Fanconi anemia - Wikipedia
Fanconi anemia (FA) is a rare, autosomal recessive, genetic disease resulting in impaired response to DNA damage in the FA/BRCA pathway.
Fanconi Anemia - StatPearls - NCBI Bookshelf
2024年6月19日 · Fanconi anemia is the most common cause of inherited bone marrow failure due to a rare autosomal recessive genetic disorder involving all 3 blood cell lines in which homozygous or heterozygous mutations result in pathogenic alleles, including point mutations, duplications, splicing defects, and deletions.[1]
Fanconi Anemia: Causes, Symptoms, Diagnosis, Treatment - WebMD
2024年8月3日 · Fanconi anemia is a recessive gene disorder that causes anemia. Learn how it’s treated and if you can prevent it.
Fanconi anemia - MedlinePlus
Fanconi anemia is a condition that affects many parts of the body. People with this condition may have bone marrow failure, physical abnormalities, organ defects, and an increased risk of certain cancers. The major function of bone marrow is to produce new blood cells.
Fanconi Anemia - Symptoms, Causes, Treatment | NORD
Fanconi anemia (FA) is a rare genetic disorder, in the category of inherited bone marrow failure syndromes. Half the patients are diagnosed prior to age 10, while about 10% are diagnosed as adults.
Fanconi Anemia - GeneReviews® - NCBI Bookshelf
2002年2月14日 · Fanconi anemia (FA) is the most common genetic cause of aplastic anemia and one of the most common genetic causes of hematologic malignancy. The ratio of males to females is 1.2:1 (p<0.001 vs expected 1.00).
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