Brunner Syndrome

Overview

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

Available Treatments (0)

Clinical Presentation

Signs and symptoms associated with Brunner Syndrome, sourced from HPO and Orphanet clinical annotations.

Classification & Codes