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Chronic Immune Thrombocytopenic Purpura in Monozygotic Twins — Genetic Factors Predisposing to ITP

List of authors.
  • Andrew J. Laster, M.D.,
  • C. Lockard Conley, M.D.,
  • Thomas S. Kickler, M.D.,
  • Carole A. Dorsch, M.D.,
  • and Wilma B. Bias, Ph.D.

Chronic immune thrombocytopenic purpura (ITP) appeared in monozygotic twin girls during adolescence. An older sister was discovered to have less severe thrombocytopenia without purpura. Increased amounts of platelet-associated immunoglobulin were detected in the proband and her sisters but in no other members of the family. Antibodies reacting with nuclear components were demonstrated in the serum of the three sisters, both parents, and other members of the kindred, some of whom had immunologically mediated clinical disorders. These observations add to the increasing evidence that a genetically determined disorder of immune regulation is often a factor predisposing to chronic ITP.The Kindred . . .

Funding and Disclosures

Supported in part by grants (P60 AM 20558 and AM 20656) from the U.S. Public Health Service.

We are indebted to Dr. J. Douglas Pinney, who supervised the initial care of the twins and kindly referred them to us.

Author Affiliations

From the Departments of Medicine and Pathology, Johns Hopkins University School of Medicine, Baltimore. Address reprint requests to Dr. Conley at the Department of Medicine, Johns Hopkins Hospital, Baltimore, MD 21205.

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