Great early druze: symptoms, causes and treatment

The most early dormitories are a situation in which an early closure of one or more draws occurs in the skull, as the closure of this druze in the skull early leads to the rise of an abnormal form of the head and in part of the cases for an imbalance in the eyelids and the facial building to compensate for the closure of this scale. The possibility of the birth of another child suffering from this phenomenon in a family has previously had a child suffering from a maximum early druze is a very small possibility, and the possibility of the birth of a child with this phenomenon for a father suffering from it is also a little possibility. Types of big druze. 2.. Metopic attachment takes the head a triangular shape forward, and the distance between the eyes is very small. 3. Coronal attachment on one side, either right or left, the structure is not symmetrical of the skull, as the early closure of one of the two ends of the coronary jam causes the front of the front of the closed side and emerges from the open side, in this case it is also caused inaccuracy in the eyes and ears. 4. Coronal suture on both sides is flat and wide from the front and the head grows to the top, this situation can arise for an unknown reason or as part of more complicated syndrome such as Crouzon syndrome and appertrom syndrome. 5. Lambodoid sutting is a foolish shape of the head that becomes more like a species as it is possible to shut down this bite on both sides or from one side and cause a flat back. Symptoms of large druze in the following clarification of the most prominent symptoms: 1. The symptoms commonly found in predominant children with a maximum early druze are no other exhibitor except twisting the shape of the skull, but there are a number of signs that may distort the problem: the head and face building. Fonticulus in the child’s head. Swelling along the closed seams. A departure from the natural growth states of the head appears during periodic tests in the mother and children’s clinic. 2.. Unusual symptoms of unpredictable signs: head pain. Loss of appetite. vomiting. Delay the growth. The causes and factors of the risk of maximizing early druze in general do not know what the reason is that leads to the closure of early druze, and as it appears that it is not a genetic phenomenon, sometimes it happens as part of the symbolism of chromosome defect that affects a number of devices in the body, and the most prominent reasons are the following. Druze, and its cause is unknown, although it is apparently a mixture of genes and environmental factors. 2. Breasted early dedicated druze due to certain genetic syndromes such as apertroms, PFFEFERFER syndrome or Crouzon syndrome, which may affect the growth of your child’s skull, these syndromes usually also contain physical features. And other health problems. The complications of the maximum premium druze In the event of non -treatment, the disease can cause the following symptoms: permanent deformation of the head and face. Poor self -state and social isolation. The risk of increasing intracranial pressure of the large early druze is small, as long as the thread and the shape of the head are surgically fastened, but children with underlying syndrome can develop an increase in intracranial pressure if their skulls do not expand enough to make room for their growing brains, as if it is not treated, the increased. Cognitive weakness. Inactivity. My father uncle. Eye movement disorders. Plugs. Dead in rare cases. The diagnosis of the maximum druze requires the maximum of the early druze an evaluation by specialists such as a neurosurgeon or a specialist in plastic and reconstructive surgery. The diagnosis of maximizing early druze may include: 1. A physical test examines the doctor’s head in search of deformities such as stitches and looking for distortions in the face. 2. Photography can show computerized tomography or magnetic resonance imaging of your child’s skull if there are stitches that are combined, and ultrasound can be used for cranial. Where the integrated stitches can be identified by its absence, because it is invisible as soon as the docking or through the bump of the dramatic line, the scan and images can also be used to make accurate measurements of the shape of the skull. 3.. Genetic tests, if your doctor suspects that basic genetic syndrome can help genetic tests to determine the syndrome. The treatment of the maximum druze is the procedure in general, a team that includes a specialist in head and face surgery, and a specialist in neurosurgery, endoscopic surgery or open surgery can be performed in the following details: laparoscopic surgery can be considered a slight severity for children up to 6 months, as is, removed. of growth of course. Compared to the open procedure, endoscopic surgery has a smaller incision, it usually includes one night in the hospital and usually does not require blood transfusion. Open surgery is performed open surgery for children older than 6 months, as the surgeon performs the following: An incision is made in the scalp and skull bones. It reforms the affected part of the skull. The skull is installed in place with absorbent panels and screws. Open surgery usually includes three or four days hospitalization and blood transfusion is usually needed, it is a one -time procedure in general, but in complex cases, many open surgeries are often needed to correct the child’s head shape. The prevention of early druze is not possible to prevent the disease.