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  Vol. 99 No. 6, June 1969 TABLE OF CONTENTS
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"Familial" Scleroderma

Kelmar M. Burge, MD; Harold O. Perry, MD; Gunnar B. Stickler, MD

Arch Dermatol. 1969;99(6):681-687.


Abstract

Two sisters with onset of scleroderma in childhood initially developed similar manifestations of the disease, with flexion deformities and subcutaneous sclerosis of the distal extremities. Twelve cases involving families with more than one member affected by scleroderma were found in the literature, and the four cases that were documented in detail are summarized. The paucity of familial reports does not appear to support, as yet, an acceptable theoretic pattern of genetic transmission.



Author Affiliations

Rochester, Minn

From the Mayo Clinic and Mayo Foundation: Section of Dermatology (Dr. Perry), and of Pediatrics (Dr. Stickler). Mayo Graduate School of Medicine (University of Minnesota), Rochester, Minn (Dr. Burge).


Footnotes

Accepted for publication Jan 3, 1969.

Reprint requests to Mayo Clinic, 200 First St SW, Rochester, Minn 55901.



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