Oral Squamous Cell Carcinoma in a Patient with Fanconi Anemia
Fanconi anemia (FA) is a rare autosomal recessive genetic disorder characterized by different types of malformations, skin lesions, bone marrow failure, and increased risk for both hematological malignancies and solid tumors, especially head and neck squamous cell carcinomas (HNSCC). FA patients may...
Saved in:
Main Authors: | Milla Huuhka, Aaro Turunen |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2021-01-01
|
Series: | Case Reports in Dentistry |
Online Access: | http://dx.doi.org/10.1155/2021/5571649 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Successful Treatment of Fanconi Anemia and T-Cell Acute Lymphoblastic Leukemia
by: Terrie Flatt, et al.
Published: (2012-01-01) -
Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis
by: Anneke B. Oostra, et al.
Published: (2012-01-01) -
A Molecular, Genetic, and Diagnostic Spotlight on Fanconi Anemia
by: Laura E. Hays, et al.
Published: (2012-01-01) -
Towards a Molecular Understanding of the Fanconi Anemia Core Complex
by: Charlotte Hodson, et al.
Published: (2012-01-01) -
Targeting the Fanconi Anemia Pathway to Identify Tailored Anticancer Therapeutics
by: Chelsea Jenkins, et al.
Published: (2012-01-01)