Work

Osler-Weber-Rendu Disease: A Rare Contributor to Recurrent Iron Deficiency Anemia

Year: 2024

Type: article

Abstract: Hereditary hemorrhagic telangiectasia (HHT), also called Osler-Weber-Rendu syndrome, is a rare genetic disorder inherited in an autosomal dominant pattern. It is marked by recurrent nosebleeds, arteriovenous malformations (AVMs), mucocutaneous telangiectasias, and often a family history of the condition. This case involves a 55-year-old woman with a prolonged history of spontaneous bleeding, particularly from lesions on her tongue, leading to chronic iron deficiency anemia. The case emphasizes the importance of considering HHT in patients with anemia and unexplained recurrent bleeding. It also underscores the value of targeted therapies and genetic counseling in managing the disorder.

Source: International Journal of Innovative Science and Research Technology (IJISRT)

DOI: 10.38124/ijisrt/ijisrt24oct1822

Authors: Kalva Suchitra Reddy, Mekala Siddhanth Kumar, Usha Topalkatti, Param Kadam

Institutions: Spartan Health Sciences University, Maharashtra Institute of Medical Education and Research

Language: English

Topic: Vascular Anomalies and Treatments

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: diamond

OpenAlex ID: W4404596681