Brunner Syndrome

info · Genetic · ICD-10: E70.8

An amino acid metabolic disorder characterized by recessive X-linked inheritance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11.

Signs and symptoms

Impulsivity
Aggressive behavior
Autism
Kinetic tremor
Low frustration tolerance
Self-injurious behavior
Headache
Intellectual disability
Motor delay
Diarrhea

Also known as: monoamine oxidase A deficiency