Albright's syndrome.

Authors

  • M. Tagliavanti
  • L. Garofalo
  • E. Bonifazi

Keywords:

Hypoparathyroidism, Cutaneous osteomas, Albright's syndrome

Abstract

Albright's disease is a rare hereditary disorder. In this article, we describe the case of a child affected by a variant of the above condition characterized by an incomplete and mild penetrance, namely by pseudo-pseudo-hypoparathyroidism with cutaneous osteoma and both statural and ponderal imbalance. Serum calcium, phosphorus and parathyroid hormo­ne were normal, whereas alkaline phosphatase was elevated. 

Published

2018-01-27

How to Cite

Tagliavanti, M., Garofalo, L., & Bonifazi, E. (2018). Albright’s syndrome. European Journal of Pediatric Dermatology, 6(3), 141–6. Retrieved from https://ejpd.migration.pkpps03.publicknowledgeproject.org/index.php/journal/article/view/1559

Issue

Section

Original articles