A new autosomal recessive lethal chondrodystrophy with congenital hydrops

Am J Med Genet. 1988 Mar;29(3):623-32. doi: 10.1002/ajmg.1320290321.

Abstract

Two sibs, the offspring of consanguineous parents, presented with severe short-limb dwarfism and distinct chondro-osseous, radiologic, and histologic appearance. The first sib presented at 30 wk with severe hydrops following fetal death; the second was detected by ultrasonography at 20 wk. Radiologic abnormalities included an unusual "moth-eaten" appearance of the markedly short long bones, bizzare ectopic ossification centers, and marked platyspondyly with unusual ossification centers. Marked extramedullary erythropoiesis was present in both fetuses, and chondro-osseous histology was characterized by marked disorganization of tissue with interspersed masses of cartilage, bone, and mesenchymal tissue. These sibs appear to have a distinct previously unreported autosomal recessive skeletal dysplasia, which can present as hydrops fetalis.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Consanguinity
  • Dwarfism / embryology
  • Dwarfism / genetics
  • Edema / embryology*
  • Female
  • Genes, Lethal*
  • Genes, Recessive*
  • Humans
  • Male
  • Osteochondrodysplasias / embryology
  • Osteochondrodysplasias / genetics*
  • Pregnancy