Cargando…
Juvenile Hemochromatosis in Iran: A Case Report with 5-Year Follow-up after Treatment
Juvenile hemochromatosis is a rare autosomal recessive disorder that typically occurs in the first to third decades of life. Its symptoms are more acute and severe than classic hemochromatosis. We describe a 27-year-old man who was referred to the gastrointestinal clinic with a probable diagnosis of...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Iranian Association of Gastroerterology and Hepatology
2016
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885614/ https://www.ncbi.nlm.nih.gov/pubmed/27252822 http://dx.doi.org/10.15171/mejdd.2016.20 |