Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Delayed diagnosis and complications of Fanconi anaemia at advanced age – a paradigm

7 Feb 2006

Abstract excerpt

Fanconi anaemia (FA) is a rare recessive DNA repair disorder clinically characterised by congenital malformations, progressive bone marrow failure and a high propensity for developing malignancies at an early age, predominantly acute myeloid leukaemia (AML) and squamous cell carcinoma. It is conceivable that a number of patients with hypomorphic mutations are not diagnosed as FA until severe complications in the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acute Lymphoblastic Leukemia research
Share to DNA Repair Mechanisms
Share to Polyomavirus and related diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 16611311
DOI: 10.1111/j.1365-2141.2006.05998.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Delayed diagnosis and complications of Fanconi anaemia at advanced age – a paradigmPMID 16611311Read ↗

Fanconi anaemia and leukaemia – clinical and molecular aspectsSemantic proximity Read ↗

Inherited aplastic anaemias/bone marrow failure syndromes.Semantic proximity Read ↗

Cancer in Fanconi anemia, 1927–2001Semantic proximity Read ↗

Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.Semantic proximity Read ↗

Catastrophic chemotherapy toxicity leading to diagnosis of Fanconi anaemia due to FANCD1/BRCA2 during adulthood: description of an emerging phenotype.Semantic proximity Read ↗

Fanconi anemia and its diagnosis.Semantic proximity Read ↗

Genotype-phenotype correlations in Fanconi anemia.Semantic proximity Read ↗

Fanconi's anaemia and related bone marrow failure syndromesSemantic proximity Read ↗

Squamous cell carcinomas of the head and neck in Fanconi anemia: risk, prevention, therapy, and the need for guidelines.Semantic proximity Read ↗

Predisposition to ALL and Solid Tumors Rather Than Bone Marrow Failure in FANCM-Associated Fanconi Anemia.Semantic proximity Read ↗

Investigation of mutations in Fanconi anemia genes and malignancy predisposition in Brazilian patients.Semantic proximity Read ↗

Myelodysplasia as the initial presentation of Fanconi's anaemia in a phenotypically normal child.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.