Brunner Syndrome
amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has material basis in mutation in the MAOA gene on chromosome location Xp11
en-GB/bɹʌnə ˈsɪndɹəʊm/
en-US/ˈbɹʌnɚ ˌsɪndɹəm/