Schimke immuno-osseous dysplasia: a newly recognized multisystem disease

J Pediatr. 1991 Jul;119(1 Pt 1):64-72. doi: 10.1016/s0022-3476(05)81040-6.

Abstract

On the basis of five cases personally observed and one previously reported, we describe a disorder characterized by skeletal dysplasia, rapidly progressive nephropathy, episodes of lymphopenia, and pigmentary skin changes. Defects of T-cell function were compatible with an autoimmune process. The disorder is probably of genetic origin and inherited as an autosomal recessive trait.

Publication types

  • Case Reports

MeSH terms

  • Antigens, CD / analysis
  • Autoimmune Diseases / congenital
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology
  • Bone Diseases, Developmental / complications*
  • Bone Diseases, Developmental / genetics
  • Bone Diseases, Developmental / immunology
  • Bone and Bones / pathology
  • Child
  • Child, Preschool
  • Dwarfism / complications*
  • Dwarfism / genetics
  • Dwarfism / immunology
  • Female
  • Humans
  • Kidney Failure, Chronic / complications*
  • Kidney Failure, Chronic / genetics
  • Kidney Failure, Chronic / immunology
  • Leukocyte Count
  • Male
  • Pigmentation Disorders / complications*
  • Pigmentation Disorders / genetics
  • Pigmentation Disorders / immunology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / physiology

Substances

  • Antigens, CD