HLA haplotype segregation and ultrastructural study in familial immotile-cilia syndrome

Hum Genet. 1992 May;89(3):270-4. doi: 10.1007/BF00220538.


The immotile-cilia syndrome (ICS) is a congenital disorder characterized by dysmotility or even complete immotility of the cilia in the ciliated epithelia. The most frequent consequences include recurrent airway infections from early childhood. Neonatal asphyxia often occurs. Males are usually sterile, whereas females may be fertile or infertile. The disease is inherited as an autosomal recessive trait, but previous attempts to localize the ICS susceptibility gene have so far been unsuccessful. Here, we present the case of two sib pairs affected by ICS from two unrelated families. The electron microscopic investigation of nasal biopsies showed structural anomalies of the cilia, characterized by single microtubules or doublets, arranged randomly in the axoneme. Histocompatibility antigen (HLA)-genotyping of all family members revealed: 1) a significant association of ICS with the HLA-DR7; DQW2 haplotype, which is shared by all the affected sibs (P = 0.0099; RR = 25.94); 2) a possible linkage of the ICS susceptibility gene with HLA, both the affected sibs being HLA-identical, the healthy brother in family B being HLA-different (sib-pair analysis: P less than 0.001).

MeSH terms

  • Child, Preschool
  • Cilia / pathology
  • Cilia / ultrastructure*
  • Ciliary Motility Disorders / diagnostic imaging
  • Ciliary Motility Disorders / genetics*
  • Ciliary Motility Disorders / pathology
  • Female
  • Genes, MHC Class II
  • Genetic Linkage / genetics*
  • HLA-DQ Antigens / genetics*
  • HLA-DR7 Antigen / genetics*
  • Humans
  • Male
  • Microscopy, Electron
  • Pedigree
  • Radiography


  • HLA-DQ Antigens
  • HLA-DQ2 antigen
  • HLA-DR7 Antigen