Literature DB >> 15139958

Recurrent aphthous ulcers in Fanconi's anaemia: a case report.

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.

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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


  1 in total

1.  Dental Perspective of Rare Disease of Fanconi Anemia: Case Report with Review.

Authors:  Mridula Goswami; Urvashi Bhushan; Manoj Goswami
Journal:  Clin Med Insights Case Rep       Date:  2016-03-17
  1 in total

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