A Further Case Supporting CCNK as a Neurodevelopmental Disease Gene
Clara Xiol1, Jonathan Olival2, Loreto Martorell1,3
1Department of Laboratory, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.
Clinical Genetics
|October 16, 2025
Abstract
None:
De novo CCNK missense variant associated with mild intellectual disability, subtle dysmorphism (hypertelorism, depressed/broad nasal bridge), and ventriculomegaly. This case broadens the clinical spectrum of CCNK-related neurodevelopmental disease and supports cyclin K as a disease gene; imaging and phenotype suggest a milder presentation compared with deletions.
Keywords:
CCNKgenotype–phenotype variabilityintellectual disabilityventriculomegalywhole‐exome sequencingMore Related Videos
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