Kabuki Syndrome
Journal of Pediatric Case Reports · Vol. 1, Issue 1 · pp. 1–3
Published October 1, 2025
Abstract
Kabuki syndrome is a rare congenital disorder with a predilection for affecting the skeletal, gastrointestinal, and cardiovascular systems, as well as causing intellectual disability and developmental delay. Key imaging findings include skeletal findings such as craniofacial and inner ear abnormalities. These radiological findings can be further complemented with physical examination and genetic testing in establishing a diagnosis. Although there is no cure, treatment is focused on addressing the quality of life for patients, including symptomatic management.
Keywords: genetic syndrome, congenital heart disease, congenital eye anomalies
Citation
. Kabuki Syndrome. Journal of Pediatric Case Reports. 2025;1(1):1-3. doi:10.37549/JPCR-25-0001.
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