Juvenile hemochromatosis, genetic study and long-term follow up after therapy
Middle East Journal of Digestive Diseases. 2014; 6 (2): 87-92
em Inglês
| IMEMR
| ID: emr-195232
ABSTRACT
BACKGROUND:
Hereditary hernochrornatosis [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 hernochrornatosis [JH] with a detailed molecular study of the family members
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Índice:
IMEMR (Mediterrâneo Oriental)
Idioma:
Inglês
Revista:
Middle East J. Dig. Dis.
Ano de publicação:
2014
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