ciliary

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cil·i·ar·y

 (sĭl′ē-ĕr′ē)
adj.
1. Of, relating to, or resembling cilia.
2. Of or relating to the ciliary body and associated structures of the eye.

ciliary

(ˈsɪlɪərɪ)
adj
1. (Zoology) of or relating to cilia
2. (Anatomy) of or relating to the ciliary body

cil•i•ar•y

(ˈsɪl iˌɛr i)

adj.
1. pertaining to various anatomical structures in or about the eye.
2. pertaining to cilia.
[1685–95]
ThesaurusAntonymsRelated WordsSynonymsLegend:
Adj.1.ciliary - relating to the ciliary body and associated structures of the eye
2.ciliary - of or relating to cilia projecting from the surface of a cell
3.ciliary - of or relating to the human eyelash
Translations

ciliary

[ˈsɪlɪərɪ] adj (Anat) → ciliare

cil·i·ar·y

n. ciliar, rel. a las pestañas o al párpado.
References in periodicals archive ?
In addition, POL6014 may show therapeutic benefit for a range of neutrophilic pulmonary diseases with high medical need such as non-cystic fibrosis bronchiectasis, alpha-1 antitrypsin deficiency or primary ciliary dyskinesia.
Lucy Dixon was born with a rare disease, primary ciliary dyskinesia, which means her organs are in mirror image and she catches infections regularly
Primary ciliary dyskinesia (PCD) is a rare genetic disorder involving number of human organs like upper and lower respiratory tract, spermatozoa in male and fallopian tube in females.
Approximately one half of patients with primary ciliary dyskinesia are having Kartagener syndrome.
Primary ciliary dyskinesia syndrome, or immotile cilia syndrome, is a heterogeneous collection of rare autosomal recessive disorders characterized by defects in the structure and function of cilia, leading to CRS with polyps and recurrent infections.
These successes were followed by Marfan syndrome and the Primary Ciliary Dyskinesia NGS panels.
These include such conditions as polycystic kidney disease, retinitis pigmentosa in the eye, and rare inherited disorders such as Alstrom syndrome, Bardet-Biedl syndrome, primary ciliary dyskinesia and nephronopthisis.
Congenital bronchiectasis can be exemplified by a condition known as Kartagener's syndrome, also known as primary ciliary dyskinesia syndrome, in which the patient displays situs inversus, chronic sinusitis, and bronchiectasis.
Incidence of congenital heart defects is more (95%) with situs inversus incompletes 25% of individuals with situs inversus have primary ciliary dyskinesia.
They address diseases like Marfan and Goodpasture's syndromes, sarcoidosis, autoimmune pulmonary alveolar proteinosis, hereditary haemorrhagic telangiectasia, Hermansky-Pudlak syndrome, primary ciliary dyskinesia, cystic fibrosis, scleroderma lung disease, and alpha-1 antitrypsin deficiency, and their epidemiology, genetic basis and molecular pathogenesis, animal models, clinical presentation, diagnosis, conventional management and treatment strategies, and future therapies and directions.
These ultrastructural features are consistent with complete ciliary aplasia which is a rare form of primary ciliary dyskinesia.