What is Saethre-Chotzen syndrome?

Saethre-Chotzen syndrome (SCS) is a disorder in which the symptoms are caused by premature bones in the skull. This results in a face that may seem asymmetrical for various reasons. It is relatively rare, although some doctors suspect it may be more common than the idea; Its symptoms can be so mild that it can be undiagnosed. It seems that SCS affects boys and girls-and all races-in the same number and although rare, it is the most common of the group of bone skull. Saethre wrote an article in 1930 describing the syndrome in a woman in Norway and her two children. Chotzen from Germany described a family with similar characteristics in 1931. Eyes are often crossed like Well. The nose may seem pointed and it is often said that they resemble a beak and ears are often smaller than usual and are located lower than usual on the head. The upper jaw does not fully develop and the hairline starts at the forehead very low. Although most of the symptoms are related to the face and skull, this syndaOM can also cause strap of fingers and fingers.

Physical properties aside, patients with SC generally have normal intelligence, although there is an occasional mild mental retardation. Patients with SC tend to be shorter than average, but have a normal life expectancy. There is no treatment of the syndrome itself, although some patients may require surgery to change some of their facial features, especially if the eyes are seriously affected. If operation is necessary, it most likely happens when the patient is young, usually between 9 months and 12 months.

Saethre-chotzen syndrome is inherited diseases. Only one parent must bear the disease for the child to inherit it. This means that there is a 50 % chance that the parent will give the disease to their child. Although SCS has been commonly confused with similar syndromes, a simple blood test can now definitely tell doctors whether the patient has a SCS or someA syndrome that affects the production of the skull. Patients with Saethre-Chotzen syndrome should be treated and monitored by doctors who specialize in craniophial disorders.