| Literature DB >> 15139958 |
Feyza Otan1, Gokhan Açikgöz, Umur Sakallioglu, Burcu Ozkan.
Abstract
Fanconi's anaemia (FA) is an autosomal recessive disorder that is clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, and an increased predisposition to malignancies. Patients with FA often present with bleeding and infection, which are symptoms related to thrombocytopenia and neutropenia. There are few reports of the oral manifestations of FA. We describe oral aphthous ulcerations in two siblings with FA. There was a rapid improvement and healing of ulcers after blood transfusions and increased haemoglobin levels. This may support the role of severe anaemia in oral ulcerations.Entities:
Mesh:
Year: 2004 PMID: 15139958 DOI: 10.1111/j.1365-263X.2004.00549.x
Source DB: PubMed Journal: Int J Paediatr Dent ISSN: 0960-7439 Impact factor: 3.455