Craniodysplasia

Craniodysplasia (synonyms: acrodisia, trigonocephaly, syndactylic cranioplyornothy) is a rare congenital hereditary disease characterized by disturbances in the development of the skull bones, facial bones and cartilage, which leads to deformation of the patient’s head and face.

The causes of craniodyspasia are not fully understood, however, as a rule, they are observed in the presence of heredity for this disease, especially if parents have similar problems.

Symptoms of craniodisposition may include: 1. Elongated and pointed head shape 2. Reduced distance between the eye sockets

Craniodysplasia or acrodysplasia refers to one of the shapes of the cranium (skull) of a child during infancy. This pathology refers to a number of anomalies associated with the development and growth of the bones of the skull. A distinctive feature of this state is the manifestation of a brighter, more violent

Craniodysplasia is a rare congenital disease in which congenital changes occur in the bones of the child’s skull. Problems with the bones of the skull can lead to various defects, such as premature birth, facial asymmetry, deafness, etc.

If the bones of the cranial vault are affected, abnormal growth occurs in the front part of the skull, and an increase in the size and weight of the head in the back part. As a result, various defects arise - wide nostrils, open or wide mouth, sunken nose, protruding jaw. Many children with craniodyspasia have hearing problems. They hear sounds from the top of their heads, which lead to the development of tinnitus. In this case, the child may not even know that he has a problem.