Wolcott-Rallison syndrome: Diabetes mellitus and spondyloepiphyseal dysplasia

H. Stöß, H. J. Pesch, B. Pontz, A. Otten, J. Spranger

Research output: Contribution to journalArticlepeer-review

61 Scopus citations

Abstract

In 1972, Wolcott and Rallison described three siblings with a combination of infancy-onset diabetes mellitus and multiple epiphyseal dysplasia. We have observed a brother and sister with the same disorder. The chondro-osseous lesions are those of a spondylo-epiphyseal dysplasia. The diabetes mellitus is relatively mild. Histologic and electron microscopic studies of chondro-osseous tissue show findings similar to those in other epiphyseal and spondylo-epiphyseal dysplasias. In addition, however, atypical collagen-like fibres are found inside and outside chondrocytes. Collagen production seems to be normal in cultured fibroblasts. From the available data it appears that the association of characteristic chondro-osseous and endocrine abnormalities is non-random and that the lesions are independent manifestations of a pleiotropic gene. We propose to call this disorder the Wolcott-Rallison Syndrome.

Original languageEnglish
Pages (from-to)120-129
Number of pages10
JournalEuropean Journal of Pediatrics
Volume138
Issue number2
DOIs
StatePublished - Mar 1982
Externally publishedYes

Keywords

  • Bone dysplasia
  • Diabetes mellitus
  • Growth
  • Small stature
  • Spondylo-epiphyseal dysplasia

Fingerprint

Dive into the research topics of 'Wolcott-Rallison syndrome: Diabetes mellitus and spondyloepiphyseal dysplasia'. Together they form a unique fingerprint.

Cite this