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      Wolcott-Rallison syndrome: diabetes mellitus and spondyloepiphyseal dysplasia.

      European Journal of Pediatrics
      Biopsy, Bone Diseases, Developmental, complications, pathology, Bone and Bones, Cells, Cultured, Child, Collagen, biosynthesis, Diabetes Mellitus, Type 1, Female, Fibroblasts, metabolism, Humans, Male, Syndrome

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          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.

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