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Iatreia
versión impresa ISSN 0121-0793
Resumen
HERNANDEZ-WOODBINE, María José; CASTILLO-RIX, Daniel Sebastián del y BAQUERO-MEJIA, Ingrid Carolina. Report of a new mutation in Colombia in a patient with Kabuki Syndrome. Iatreia [online]. 2020, vol.33, n.1, pp.78-83. ISSN 0121-0793. https://doi.org/10.17533/udea.iatreia.38.
Introduction:
Kabuki Syndrome is a pediatric congenital disorder of genetic origin. These patients present morphological abnormalities such as cleft palate, prominent eyeballs, persistence of fingerpads, and vertebral abnormalities. Most also have learning difficulty.
Objective:
Report a pediatric case of Kabuki Syndrome to increase the recognition of the phenotype associated with it and the likelihood of a diagnosis with the use of a clinical case report.
Case report:
A nine-year-old male patient with clinical characteristics and probable genetic diagnosis of Kabuki Syndrome. He exhibits elongated eyelids, cleft palate, low auricular implantation, persistence of fingerpads, reduced height, and primary sclerosing cholangitis.
Conclusion:
Diagnostic suspicion of type one Kabuki Syndrome is characterized mainly by facial alterations. The following patient presents multiple distinctive characteristics described in literature. A genetic study considers the gene KMT2D a possible pathologic genetic variant of the disease.
Palabras clave : Congenital Abnormalities; Cholangitis Sclerosing; Colombia; Genetic Phenomena.