GTR Home > Conditions/Phenotypes > 15q24 deletion syndrome


The 15q24 microdeletion syndrome is characterized by global developmental delay; mild to severe (usually at least moderate) intellectual disability; facial dysmorphisms; congenital malformations of the hands and feet, eye, and genitalia; joint laxity; and growth retardation and failure to thrive. Less common findings include: seizures; conductive and sensorineural hearing loss; hypospadias and/ or micropenis. Males and females are affected equally. [from GeneReviews]

Available tests

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Associated genes

  • Location: 15q24

Clinical features


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