Variants
Sign InSign Up

Primary ciliary dyskinesia 25

Your Results

Sign In

Description

Primary ciliary dyskinesia-25 is an autosomal recessive disorder caused by defective ciliary movement. Affected individuals have recurrent upper and lower airway disease, bronchiectasis, and decreased fertility. About half of patients show laterality defects, including situs inversus totalis. Respiratory cilia from patients show defects in the inner and outer dynein arms (summary by Tarkar et al., 2013). For a general phenotypic description and a discussion of genetic heterogeneity of primary ciliary dyskinesia, see 244400.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

4

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    615482

  • Orphanet
  • HPO
  • Medgen

    C3809641

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard