Fanconi's anemia

(redirected from Fanconi anemia)
Also found in: Dictionary, Medical, Acronyms, Encyclopedia, Wikipedia.
Graphic Thesaurus  🔍
Display ON
Animation ON
Legend
Synonym
Antonym
Related
  • noun

Synonyms for Fanconi's anemia

References in periodicals archive ?
Additionally, the report provides an overview of key players involved in therapeutic development for Fanconi Anemia and features dormant and discontinued projects.
The findings also create a bit of molecular intrigue--namely, how cells used in the study that still had the Fanconi anemia (FA) DNA repair defect recovered and grew normally after targeted treatment.
D'Andrea, "How the fanconi anemia pathway guards the genome," Annual Review of Genetics, vol.
Ocular and orbital manifestations of the inherited bone marrow failure syndromes: Fanconi anemia and dyskeratosis congenita.
Better posttransplant outcome with fludarabine based conditioning in multitransfused fanconi anemia patients who underwent peripheral blood stem cell transplantation.
Comparative study of Fanconi anemia in children of different ethnic origin in South Africa.
He also suffers from Fanconi anemia, a rare disease that often leads to cancer.
It also reviews key players involved in the therapeutic development for Fanconi Anemia.
All five types of Fanconi Anemia, a red and white blood cell and platelet deficiency, are inherited, but Type C is the most common.
Enter the Institute for Justice, which in 2009 filed suit on behalf of a group of patients, including Lewiston, Maine mother Doreen Flynn, three of whose children are afflicted with a blood disease called Fanconi anemia.
On Friday, January 27, Wildes was finally able to meet the girl whose life he saved, a six-year-old Evansdale, Towa, girl who suffered from Fanconi anemia, an extremely rare genetic blood disorder that attacks the bone marrow.
Most common causes reported in children are aplastic anemia, megaloblastic anemia, infections like malaria, enteric fever, leishmaniasis, Fanconi anemia, malignancies like acute lymphoblastic leukemia and myelodysplasia.
In addition to serving its clientele, SYSTEMATICS and its 30 employees are staunch supporters of several community non-profit organizations, including the Shrewsbury American Youth Football and Cheer Organization, which serves hundreds of the area's young athletes, Coley's Cause, which raises funds for fighting the orphan disease Fanconi Anemia, and the Tufts Health Plan 10K for Women.
Samantha and David, 37, found when their daughter Jessica was nine that she had the rare condition Fanconi Anemia (FA).
Full browser ?