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  Vol. 107 No. 2, Feb 1961 TABLE OF CONTENTS
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The Milk-Alkali Syndrome

MAJOR RUSSELL E. RANDALL, JR., USAF (MC); MAURICE B. STRAUSS, M.D.; WILLIAM F. McNEELY, M.D.

Arch Intern Med. 1961;107(2):163-181.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

I. The Diversity of Clinical Manifestations

Eleven years ago Burnett and his associates1 described a syndrome occurring in patients who had ingested milk and absorbable alkali for prolonged periods of time. The characteristic features were hypercalcemia without hypercalciuria or hypophosphatemia, mild alkalosis, a normal serum alkaline phosphatase, severe renal insufficiency with azotemia, and calcinosis manifested chiefly by the presence of band keratopathy. Improvement followed restriction of the intake of milk and absorbable alkali. In the intervening decade it has become apparent that there are many variants in the "milk-alkali syndrome," as it has now come to be known.2-20 It is the purpose of this paper to present 4 cases illustrating the variability of manifestations which may result from excessive intake of milk and to stress 3 facts: 1. Hypercalcemia may continue for many months after cessation of a large calcium intake; 2. Moderate impairment in renal function with . . . [Full Text PDF of this Article]


Author Affiliations

BOSTON

From the Medical Service and Research Laboratory, Boston Veterans Administration Hospital, and the USAF Hospital, Travis Air Force Base, California, and the Departments of Medicine, Boston University School of Medicine and Tufts University School of Medicine, Boston.


Footnotes

Submitted for publication April 13, 1960.

Requests for reprints should be addressed to: Secretary, Research Laboratory, Boston Veterans Administration Hospital, 150 South Huntington Ave., Boston (30).



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