What is Hallermann Streiff's syndrome?

Extremely rare genetic state, Hallermann Streiff's syndrome is primarily indicated by a dwarf, abnormalities in the development of skull and dental, thin hair and vision problems. It is also known as Francois Dyscephaly. Because there is no medicine for Hallermann Streiff's syndrome; It can only treat a team of specialists - such as dentists, optometists and surgeons - for relief from symptoms. There was no known cause for the syndrome

Hallermann Streiff's syndrome can be marked with visual tracks, including a small lower jaw, a tight nose that looks similar to a beak and a wide head. Individuals with this disease are usually short, but adequate. The eyes are often unusually small. In some cases the teeth will be present at birth. Visual problems are usually present when the individual is born and usually consists of caratet and possible eye damage due to the small size of the eye. In rare cases, the condition may also cause mental retardation.

Deformities in the structure of the airways and the skull of individuals with disease can lead to other diseases. There is also potential for obstructive sleep apnea, problems with feeding and pulmonary infections. Extra teeth in the jaw can cause malformation and crowd.

It has been speculated that Hallermann Streiff's syndrome is due to gene mutation due to recessive characteristics in both parents. In most reported cases, the development of the state is random; Usually there is no family history of the disease. Studies have focused on trying to find out what event or many events causes disease development.

The syndrome must usually be diagnosed after birth, although some signs, such as the insufficiently developed jawd, have been inflated in ultrasound. Physical examination will provide doctors most of the information necessary to determine whether the patient has a condition. X -rays can also be useful because deformed bones are one of KLíčových indicators of the disease.

Hallermann Streiff's syndrome acquires its name by Wilhelm Hallermann and Enrica Streiff, men who have presented the first reports of patients with the condition. The medical community discovered it at the end of the 18th century. Today the organization known as Schantenkinder E.V. In Germany, it offers support for individuals.