Add to ORKGFanconi anaemia (FA) is an inherited genetic disorder characterised by somatic anomalies, bone marrow failure and an increased predisposition to solid tumours and haematological malignancies. South African (SA) black and Afrikaner individuals are at higher than average risk for this condition owing to genetic founder mutations in certain Fanconi-associated genes. This review explores the epidemiology, clinical presentation, diagnostic modalities and recommended care of affected patients, focusing on the founder population groups in SA. The early diagnosis of FA is important and provides improved opportunities for early intervention, but remains challenging
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anaemia (FA) is a recessive autosomal disease determined by mutations in genes of at least e...
Fanconi anemia (FA) is an autosomal recessive genetic disease characterized by progressive bone marr...
Fanconi anaemia (FA) is an inherited genetic disorder characterised by somatic anomalies, bone marro...
Fanconi anaemia (FA) is an inherited genetic disorder characterised by somatic anomalies, bone marro...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Fanconi Anemia (FA) is a rare autosomal recessive disorder affecting multiple body systems. The diag...
Fanconi anaemia is a rare genetic disorder which leads to bone marrow failure and results in decreas...
Populations in North Africa (NA) are characterized by a high rate of consanguinity. Consequently, th...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
Fanconi anemia (FA) is characterized by bone marrow failure, malformations, and chromosome fragility...
Introduction: Fanconi Anaemia (FA) is an autosomal recessive disorder characterized by defects in DN...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
BACKGROUND : Fanconi anemia (FA) is phenotypically diverse, hereditary condition associated with bon...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anaemia (FA) is a recessive autosomal disease determined by mutations in genes of at least e...
Fanconi anemia (FA) is an autosomal recessive genetic disease characterized by progressive bone marr...
Fanconi anaemia (FA) is an inherited genetic disorder characterised by somatic anomalies, bone marro...
Fanconi anaemia (FA) is an inherited genetic disorder characterised by somatic anomalies, bone marro...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Fanconi Anemia (FA) is a rare autosomal recessive disorder affecting multiple body systems. The diag...
Fanconi anaemia is a rare genetic disorder which leads to bone marrow failure and results in decreas...
Populations in North Africa (NA) are characterized by a high rate of consanguinity. Consequently, th...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
Fanconi anemia (FA) is characterized by bone marrow failure, malformations, and chromosome fragility...
Introduction: Fanconi Anaemia (FA) is an autosomal recessive disorder characterized by defects in DN...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
BACKGROUND : Fanconi anemia (FA) is phenotypically diverse, hereditary condition associated with bon...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anaemia (FA) is a recessive autosomal disease determined by mutations in genes of at least e...
Fanconi anemia (FA) is an autosomal recessive genetic disease characterized by progressive bone marr...