Hypoparathyroidism in Wilson's Disease
Document Type
Letter
Publication Date
3-15-1984
Description
To the Editor: We enjoyed Dr. Scheinberg's perceptive editorial (Oct. 13 issue) on the value of investigating rare diseases.1 Elucidation of the mechanism of Wilson's disease and the subsequent successful treatment of this condition with penicillamine may also have shed considerable light on the etiologic mechanism of a rare birth defect, Ehlers–Danlos syndrome (dermatorrhexis cutis hyperelastica). This defect, which occurs spontaneously as a probable result of mendelian inheritance, also appears to be associated with maternal use of penicillamine in pregnancy.2 Penicillamine inhibits condensation of soluble tropocollagen because of affinity to the aldehyde. It chelates with unbound copper as well as.
Citation Information
Piper, Joyce M.; Rosa, Franz W.; Lanska, Douglas; Lanska, Mary Jo; Hoffman, Raymond G.; Rimm, Alfred A.; Lebow, Robert; Carpenter, Thomas O.; Carnes, David L.; Anast, Constantine S.; and Scheinberg, I. Herbert. 1984. Hypoparathyroidism in Wilson's Disease. New England Journal of Medicine. Vol.310(11). 727-728. https://doi.org/10.1056/NEJM198403153101123 PMID: 6700655 ISSN: 0028-4793