Cleoparanial dysostosis, also known as kleidocranial dysplasia, is a very rare genetic and hereditary malformation, as there is a delay in the development of the human brain and the region of children and patients.
While there may be several cases of this condition in the same family, generally the characteristics and symptoms that occur vary from person to person and each case should be evaluated by the pediatrician.
- The characteristics of kleidocannial dysplasia vary considerably from person to person.
- However.
- The most common include:.
The baby’s spring delay was the baby’s fontanelle;
Featured Menton and Front;
Very curious nose;
The mouth tastes more than normal;
Defective or missing collarbones;
Straight and very flexible limbs;
Delay in tooth growth
In addition, dysplasia can also affect the spine and in these cases other problems such as scoliosis and low stature, for example, may occur. Similarly, changes in the face can cause changes in the sinuses, which can lead to a more frequent sinus attack. in children.
Diagnosis of kleidocannial dysplasia, usually made by the pediatrician, after observing the characteristics of the disease, for this reason, it may be necessary to pass diagnostic tests, such as x-rays, to confirm changes in the blood in the chest, for example.
Kleoparanial dysplasia is more common in children whose two priests have malformations, however, as is caused by genetic alteration, it is conditional, it could occur in the face of people who do not raise other cases in the family, because of a family. Genetic mutation.
However, kleidocannial dysplasia is very rare, there is only one case out of every 1 million births in the world.
In many cases, a type of treatment is not necessary to correct changes caused by kleidocannial dysplasia, due to the child’s development to have a good quality of life.
However, in the case of major malformation, it is common for your doctor to recommend different types of treatment depending on the change to be treated:
In case of problems and dental changes, the goal is to improve the appearance of the mouth to allow the child to develop more confidently, in addition to having greater ease of chewing food.
This way, it’s important to see a dentist or orthodontist to assess needs, such as placing a certain type of device in your surgery.
Due to changes in the face and patients, some children with kleidocannial dysplasia may have difficulty speaking correctly. In addition, the pediatrician may indicate conducting speech therapy sessions.
Because sinusitis is relatively common in the patient with this condition, your doctor may indicate which of the first warning signs of sinusitis, such as irritation, presence of mild rhinitis, how to properly start treatment, as quickly as possible, and help with recovery.
For kleidocannial dysplasia that causes weakness in patients, your doctor may advise taking calcium and vitamin D supplements, for example.
In addition, it is important to regularly help your pediatrician and orthopedic surgeon assess whether there are new complications to treat to improve a child’s quality of life.