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  Vol. 52 No. 2, August 1936 TABLE OF CONTENTS
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CALCINOSIS UNIVERSALIS AND CALCINOSIS CIRCUMSCRIPTA IN INFANCY AND IN CHILDHOOD

THREE CASES OF CALCINOSIS UNIVERSALIS, WITH A REVIEW OF THE LITERATURE

JACOB L. ROTHSTEIN, M.D.; SARA WELT, M.D.

Am J Dis Child. 1936;52(2):368-422.

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

Calcinosis is the term applied to the abnormal deposition of calcium salts in the skin, subcutaneous tissues, muscles and tendons of the body. The first authentic case was reported in association with scleroderma by Weber in 1878, who interpreted the condition as a form of gout. Since then, the syndrome has been the subject of a great deal of discussion and controversy as to the etiology, the pathology and the therapy concerned.

REVIEW OF THE LITERATURE

Calcinosis has been recognized as not being limited to any one disease and has been reported in association with a variety of conditions: scleroderma (Langmead; Tisdall and Erb; Pollitzer; Bayless; Delherm, Morel-Kahn and Coupout; Durham; Bruusgaard), scleroderma with sclerodactylia (Merklen and Vallette; Bertolotti; Olson; Thibierge, Spillman and Weissenbach; von Bernuth, case 2), scleroderma with Raynaud's disease (Hunter; Paisseau, Schaeffer and Scherrer), sclerodactylia alone (Scholefield and Weber), sclerodactylia with Raynaud's disease (Davis), Raynaud's disease alone . . . [Full Text PDF of this Article]


Author Affiliations

NEW YORK

From the Pediatric Service of Dr. Béla Schick, the Mount Sinai Hospital.



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