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Up to: Partial deletion of the short arm of chromosome 16 · Hao-Fountain syndrome
Hao-Fountain syndrome due to 16p13.2 microdeletion
A partial deletion of the short arm of chromosome 16 characterized by developmental delay, intellectual disability, speech delay, autism spectrum disorder, epilepsy, hypogonadism, and hypotonia. The behavioral profile includes impulsivity, compulsivity, stubbornness, manipulative behaviors, temper tantrums, and aggressive behaviors.
This condition has no sub-types.