Clinical presentation of a patient with congenital polycythemia.
نویسندگان
چکیده
The authors describe a 19 year old male with an isolated but absolute erythrocytosis with iron deficiency without evidence for polycythemia vera as well as another causes of erythrocytosis. The polycythemia was due to a recently described von Hippel-Lindau (VHL) mutation. By stopping iron therapy there was no more requirements for phlebotomy in this patient.
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عنوان ژورنال:
- Collegium antropologicum
دوره 30 1 شماره
صفحات -
تاریخ انتشار 2006