Ciliopathies

Ciliopathies refer to diseases due to malfunctioning cilia (singular: cilium). Cilia are organelles that are external extensions of the cell membrane. Cilia fall into two main types: primary (or immotile) cilia and motile cilia. 

Primary cilia are found in virtually every cell type, resulting in a wide range of anomalies, including central nervous system, eye, heart, kidney, liver, and skeletal abnormalities. 

Ciliopathies are caused by malfunctioning cilia. Primary cilia have important roles in cell signalling, transduction of sensory stimuli, and cell cycle control.  Motile cilia are restricted to a few specialized tissues including cells of the respiratory tract, the ependyma of the ventricles and cisterns of the CNS, spermatozoa, and the Fallopian tubes. Motile cilia are also important during embryogenesis.

There are a number of ciliopathies that can be broadly classified as being either due to motile or primary cilia malfunction. See individual articles for in-depth discussions.

Cilopathies have a varied radiological appearance and some appear more commonly than others in radiological practice. For example, autosomal dominant polycystic kidney is a ciliopathy that may be occasionally encountered in most departments, while others such as Meckel-Gruber syndrome or short ribs polydactyly syndrome may only be encountered in specialist obstetrics imaging centres.

Cilium is Latin for eyelash.

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Article information

rID: 57786
System: Paediatrics
Synonyms or Alternate Spellings:
  • Ciliopathy
  • Cilia-related disease

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