Congenital squint syndrome

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The congenital squint syndrome (also: early childhood squint syndrome ) is a congenital disorder of the eye movement , which consists of an extensive complex of symptoms. In addition to the full picture of this disease, all conceivable combinations down to individual symptoms are possible. Because of the difficult festzustellenden in practice manifestation timing, a distinction is usually due to the history of the congenital from early childhood squint beginning, which means the period from 2 to 7 months of age.

Symptoms

Fluctuating squint angles

With congenital squint, there is a large, constant squint angle, while with early childhood manifestation the squint angle is large, but usually variable. Fixation by adduction is preferred in both cases .

Nystagmus

There is still a jerk nystagmus from Latenstyp . The neutral zone, i.e. the position in which the eye tremors are calmest, is in adduction. Often a manifestation is found when covering an eye and attempting an abduction movement.

Vertical disturbances

Often there are errors in the innervation pattern of the straight and oblique eye muscles . Here significant Inkomitanzen are the horizontal variations in construction and downgaze (A / V symptoms), and the typical slant height squint.

Dissociated squint

The non-leading eye deviates upwards without recognizable regularities and to varying degrees.

Compensatory head postures

In combination with nystagmus in particular, there is often a forced head posture.

therapy

The respective treatment options are documented in the main articles. If the full picture of this disease is present, a complete cure cannot be expected. Even intensive pleoptic and orthoptic treatment procedures are often unable to bring about normal binocular vision .

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