PEDIATRICS Vol. 9 No. 3 March 1952, pp. 290-294
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EXOGENOUS HEMOCHROMATOSIS IN MEDITERRANEAN ANEMIA

ABRAHAM M. FRUMIN M.D.1, SYDNEY WALDMAN M.D.1, and PAUL MORRIS M.D.1

1 The Departments of Research and Pediatrics, Mt. Sinai Hospital, Philadelphia.

A patient with Mediterranean anemia who received many blood transfusions over a period of years is presented.

The pigment deposition in Mediterranean anemia, originally thought due to an inherited defect, is attributed to multiple blood transfusions.

It is maintained that this abnormal pigment deposition represents another instance of exogenous hemochromatosis.

Submitted on August 15, 1951


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