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Article

Emerging insights into primary ciliary dyskinesia-associated hydrocephalus: a scoping review.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 25 Sept 2025

Theochari Katerina, Kotsiou Ourania S

Abstract excerpt

Hydrocephalus, a condition caused by fluid buildup in the brain, is now recognized as a possible complication of primary ciliary dyskinesia (PCD)-a rare genetic disorder that affects the movement of tiny, hair-like structures called motile cilia. This review brings together current knowledge about the disease's causes, symptoms, and treatments. Specific gene mutations like MCIDAS, DNAH5, CCNO, and IFT46 are key...

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Identifiers

PMID: 40996446
DOI: 10.1007/s00381-025-06951-w

Genes

CCNO
DNAH5
IFT46
MCIDAS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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