https:\/\/jmg.bmj.com\/content\/early\/2023\/08\/15\/jmg-2023-109141<\/a> )<\/p>\n","protected":false},"excerpt":{"rendered":"KBG syndrome is a rare neurodevelopmental disorder caused by heterozygous variants in the ANKRD11 gene and is one of the most prevalent genetic syndromes. Many reports over the years have delineated the variable phenotypic spectrum of this condition but the skeletal and in particular the neuroimaging features remain poorly defined. We have systematically analyzed the […]<\/p>\n
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