Conductive deafness with ptosis and skeletal malformations in sibs: a probably autosomal recessive disorder

Birth Defects Orig Artic Ser. 1978;14(6B):199-204.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Blepharoptosis / genetics*
  • Bone Diseases, Developmental / genetics*
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • Genes, Recessive
  • Hearing Loss / genetics*
  • Hearing Loss, Conductive / genetics*
  • Humans
  • Infant
  • Pedigree
  • Syndrome