a rare genetic disorder characterized by
microcephaly, severe intellectual developmental disorder, obesity, seizures,
hypogonadism, and distinct facial features. Fully expressed primarily in males, it is caused by an X-linked recessive trait mutation in the
PHF6 gene. [Mats Gunnar Börjeson (1922– ), Hans Axel Forssman (1912–1994), and J. O. Orla Lehmann (1927– ), Swedish physicians]