Journal of Pediatric Case Reports

Kabuki Syndrome

Journal of Pediatric Case Reports · Vol. 1, Issue 1 · pp. 1–3

Published October 1, 2025

DOI: 10.37549/JPCR-25-0001

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

Kondapalli K, Towbin RB, Morgan D, Schaefer CM, Towbin AJ. Kabuki Syndrome. Journal of Pediatric Case Reports. 2025;1(1):1-3. doi:10.37549/JPCR-25-0001.

©Anderson Publishing, Ltd. All rights reserved. Reproduction in whole or part without express written permission is strictly prohibited.

More from Vol. 1, Issue 1

Aortic Stenosis

Fadi E. Moaikel, Richard B. Towbin, Jeffrey A. Towbin, Jason N. Johnson, Alexander J. Towbin

September 2025 · Vol. 1, Issue 1

Cystic Wilms Tumor

Reyhaneh S. Rahimi, Alexander J. Towbin, Daniel Morgan, Richard B. Towbin

September 2025 · Vol. 1, Issue 1

Thyroglossal Duct Cyst

Aaron C. Llanes, Richard B. Towbin, Carrie M. Schaefer, Alexander J. Towbin

September 2025 · Vol. 1, Issue 1

Fibromyxoid Sarcoma

Nikolas J. Tsiouplis, Richard B. Towbin, Carrie M. Schaefer, Daniel Morgan, Alexander J. Towbin

September 2025 · Vol. 1, Issue 1