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It is characterized by distinctive facial features including arched eyebrows; long eyelashes; long openings of the eyelids (long palpebral fissures) with the lower lids turned out (everted) at the outside edges; a flat, broadened tip of the nose; and large protruding earlobes. 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Ancestor membership does not transfer phenotype values between groups.","importantHtml":""},"sections":[{"bodyHtml":"<p>Kabuki syndrome is caused by variants (also known as mutations) in the KMT2D gene (also known as MLL2) or the KDM6A gene.</p><p>Between 55 and 80 percent of cases of Kabuki syndrome are caused by variants in the KMT2D gene. This gene provides instructions for making an enzyme, called lysine-specific methyltransferase 2D, that is found in many organs and tissues of the body. Lysine-specific methyltransferase 2D functions as a histone methyltransferase. Histone methyltransferases are enzymes that modify proteins called histones. Histones are structural proteins that attach (bind) to DNA and give chromosomes their shape. By adding a molecule called a methyl group to histones (a process called methylation), histone methyltransferases control (regulate) the activity of certain genes. Lysine-specific methyltransferase 2D appears to activate certain genes that are important for development.</p><p>Between 2 and 6 percent of cases of Kabuki syndrome are caused by variants in the KDM6A gene. This gene provides instructions for making an enzyme called lysine-specific demethylase 6A. This enzyme is a histone demethylase, which means that it helps to remove methyl groups from certain histones. Like lysine-specific methyltransferase 2D, lysine-specific demethylase 6A regulates the activity of certain genes, and research suggests that the two enzymes work together to control certain developmental processes.</p><p>The KMT2D and KDM6A gene variants associated with Kabuki syndrome lead to the absence of the corresponding functional enzyme. A lack of either of the enzymes produced from these genes disrupts normal histone methylation and impairs proper activation of certain genes in many of the body&#x27;s organs and tissues, resulting in the abnormalities of development and function characteristic of Kabuki syndrome.</p><p>Some people with Kabuki syndrome have no identified KMT2D or KDM6A gene variant. These individuals are diagnosed based on the presence of characteristic features of the condition. The cause of Kabuki syndrome in these individuals is unknown.</p><p class=\"section-source\"><a href=\"https://medlineplus.gov/genetics/condition/kabuki-syndrome/#causes\">MedlinePlus Genetics: Causes</a></p>","key":"forms","title":"What causes Kabuki syndrome?"},{"bodyHtml":"<p>People with Kabuki syndrome may have mild to severe developmental delay and intellectual disability. Affected individuals may also have seizures, an unusually small head size (microcephaly), or weak muscle tone (hypotonia). Some have eye problems such as rapid, involuntary eye movements (nystagmus) or eyes that do not look in the same direction (strabismus).</p><p>Other characteristic features of Kabuki syndrome include short stature and skeletal abnormalities such as abnormal side-to-side curvature of the spine (scoliosis), short fifth (pinky) fingers, or problems with the hip and knee joints. The roof of the mouth may have an abnormal opening (cleft palate) or be high and arched, and dental problems are common in affected individuals. People with Kabuki syndrome may also have fingerprints with unusual features and fleshy pads at the tips of the fingers. These prominent finger pads are called fetal finger pads because they normally occur in human fetuses; in most people they disappear before birth.</p><p>A wide variety of other health problems occur in some people with Kabuki syndrome. Among the most commonly reported are heart abnormalities, frequent ear infections (otitis media), hearing loss, and early puberty.</p><p class=\"section-source\">Source: <a href=\"https://medlineplus.gov/genetics/condition/kabuki-syndrome\">MedlinePlus Genetics</a></p>","key":"overview","title":"Condition overview"}],"sharedSources":[],"slug":"kabuki-syndrome","sourceDocuments":[{"name":"Kabuki syndrome","reviewed":"2013-10","sections":{"causes":{"fetchedAt":"2026-10-20T20:22:38.899039+00:00","label":"Causes","pageSha256":"247947526751aa88149a21093ad56d732413bb3da0c53d23d71ed1846a5aa4fc","sourceUrl":"https://medlineplus.gov/genetics/condition/kabuki-syndrome/#causes","status":"available"}},"source_release":"2026-10-01","url":"https://medlineplus.gov/genetics/condition/kabuki-syndrome"}],"sourceNote":"MedlinePlus descriptions and Causes; original HPO annotations.","takeawayHtml":"Cause explanations are from MedlinePlus Genetics. Feature values below retain their original sources and patient groups.","title":"Kabuki syndrome"},"schemaVersion":1}