Cargando…
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...
| Autores principales: | , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
International Scientific Literature, Inc.
2020
|
| Materias: | |
| 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 |