Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation

M. Klaassens, E. W. Blom, J. J. P. Schrander, Carrie Ris-Stalpers, A. C. Nieuwenhuijzen Kruseman, M. A. M. van Steensel, C. T. R. M. Schrander-Stumpel*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)690-694
JournalBritish Journal of Dermatology
Volume162
Issue number3
DOIs
Publication statusPublished - Mar 2010

Keywords

  • Albright hereditary osteodystrophy
  • dermal hypoplasia
  • PHP1a
  • pseudohypoparathyroidism
  • skin changes

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