Juvenile Hemochromatosis, Genetic Study and Long-term Follow up after Therapy

BACKGROUND Hereditary hemochromatosis (HH) is a very rare disease in Iran and reported cases are all negative for HFE mutation. We report a family affected by severe juvenile hemochromatosis (JH) with a detailed molecular study of the family members. METHODS We studied a pedigree with siblings affec...

Descripción completa

Detalles Bibliográficos
Autores principales: Malekzadeh, Masoud M., Radmard, Amir Reza, Nouroozi, Alireza, Akbari, Mohammad Reza, Amini, Marzie, Navabakhsh, Behrooz, Caleffi, Angela, Pietrangelo, Antonello, Malekzadeh, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Association of Gastroerterology and Hepatology 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034669/
https://www.ncbi.nlm.nih.gov/pubmed/24872867

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034669/
https://www.ncbi.nlm.nih.gov/pubmed/24872867

Ejemplares similares