Hereditary Hemorrhagic Telangiectasia in a Sickle Cell Trait Patient: A Report of a Rare Case with Use of Nuclear Medicine, and a Literature Review

Patient: Female, 49-year-old Final Diagnosis: Hereditary haemorrhagic telangiectasia Symptoms: Anemia • dyspnea • epistaxis • lipothymia • melena • weakness Medication:— Clinical Procedure: Electrofulguration Specialty: Gastroenterology and Hepatology • Genetics • Radiology OBJECTIVE: Rare disease B...

Descripción completa

Detalles Bibliográficos
Autores principales: Kang, Hye Chung, Pereira, Miguel Augusto Martins, Silva, Lucas Natã Lessa, Oliveira, Lucas Caetano, Márvila, Igor Silva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347035/
https://www.ncbi.nlm.nih.gov/pubmed/32614805
http://dx.doi.org/10.12659/AJCR.923355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347035/
https://www.ncbi.nlm.nih.gov/pubmed/32614805
http://dx.doi.org/10.12659/AJCR.923355

Ejemplares similares