Cutaneous Ossification in Pseudohypoparathyroidism
- 1 December 1971
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 104 (6), 643-647
- https://doi.org/10.1001/archderm.1971.04000240067009
Abstract
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism are now considered variants of the same disease and are referred to jointly as Albright's hereditary osteodystrophy. Cutaneous ossification may be a presenting feature in Albright's hereditary osteodystrophy. The second case of cutaneous ossification in Albright's hereditary osteodystrophy occurred in a 39-year-old woman.This publication has 5 references indexed in Scilit:
- Pseudohypoparathyroidism: defective excretion of 3′,5′-AMP in response to parathyroid hormoneJournal of Clinical Investigation, 1969
- Osteoma cutisArchives of Dermatology, 1969
- Primary Osteomas of SkinArchives of Dermatology, 1963
- Primary Osteoma Cutis and Diaphyseal AclasisArchives of Dermatology, 1962
- A CONTRIBUTION TO THE STUDY OF MYOSITIS OSSIFICANS PROGRESSIVAAnnals of Surgery, 1918