ArticleCureus2025
A Child With Cleidocranial Dysplasia Presenting With Seizure Disorder.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cleidocranial dysplasia (CCD) is a rare autosomal dominant disorder of membranous bones with characteristic radio-morphological manifestations. There is disordered ossification of the skull vault and the clavicle, leading to a wide-open anterior fontanelle, frontal bossing, persistent metopic suture, multiple wormian bones, and hypermobile shoulders. Other features are absent nasal bones, the presence of supernumerary teeth, absent ossification of the pubic rami causing pseudo-widening of the pubic symphysis, pseudo-epiphyses of metacarpals and metatarsals, short distal phalanges, and a bell-shaped thorax. CCD is a form of skeletal dysplasia that goes undetected until it presents with some of the associated complications or other diseases. We report the case of a seven-year-old girl presenting with seizure disorder to us, and a detailed clinico-radiological study showed CCD.
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