Crouzon syndrome is a syndrome of complex cranial and facial deformities caused by multiple premature closures of the cranial and facial sutures, often accompanied by increased intracranial pressure.
Crouzon first reported Crouzon’s syndrome in 1921, which is characterized by pointed, short or triangular head deformities, inverted upper and lower jaws, a prominent parrot’s beak nasal projection, shallow eye sockets, protruding eyeballs, light-blue sclera, widening of the distance between the eyes and exotropia.
The main cause of Cruz syndrome is not fully conclusive, and the main consideration is chromosomal abnormalities causing premature closure of the cranial sutures. Generally speaking, the treatment can be surgical, such as fronto-orbital advancement surgery to improve the cranial deformity.
In daily life, it should be noted that the diet should be light and nutritionally balanced. When children are found to have abnormal facial appearance, they should seek medical examination and treatment as soon as possible to avoid delaying their condition.