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Revista Médica Electrónica
versión On-line ISSN 1684-1824
Resumen
CORRALES ALONSO, Sahilí et al. Type I hereditary hemocrhomatosis. Case presentation. Rev.Med.Electrón. [online]. 2017, vol.39, n.1, pp. 91-100. ISSN 1684-1824.
Hereditary hemocrhomatosis is a genetic disease of difficult diagnosis in its early stages, caused by alterations in the iron metabolism; it leads to iron storage in several tissues and consequently to a great morbidity in affected patients. In this work, we presented the first case diagnosed by gastroenterologists in the Hospital Faustino Pérez, of Matanzas. The patient began with symptoms related with the endocrine sphere like impotence, and lost of libido and ejaculation. After finishing the correspondent studies, we arrived to the conclusion of post-pubertal hypogonadotropic hypogonadism: the patient presented hepatic enzymes elevation. He was referred to Hepatology consultation where the study was finished, confirming the diagnosis of Type I hereditary hemocrhomatosis through biopsy and genetic studies.
Palabras clave : hereditary hemocrhomatosis; cirrhosis by iron storage; iron overload.