Bergmann Syndrome

Bergman syndrome

Bergmann syndrome is a rare hereditary neuromuscular dysfunction syndrome characterized by impaired neuromuscular transmission in skeletal muscles and a congenital disorder of conduction along the nerve fibers of the spinal cord, externally manifested as disproportionate separation of the limbs. The syndrome belongs to the group of hereditary neuromuscular diseases and is accompanied by a delay in the formation of gait and fine motor skills. Most often it occurs in male children, but the risk of detection in women cannot be excluded and they can be carriers of the syndrome. Mostly in pathology it is detected as spontaneous