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ICD-10: Q99.8
ORPHA: 3306
These children are born with an extra chromosome, a so-called marker chromosome, which contains genetic material from chromosome 15.
General symptoms: People with marker chromosome 15 syndrome often have intellectual disabilities, low muscle tension, poor locomotor development, autism spectrum disorder and sometimes epilepsy. Many of those affected have stomach and intestinal disorders.
People with marker chromosome 15 syndrome often have intellectual disabilities, low muscle tension, poor locomotor development, autism spectrum disorder and sometimes epilepsy. Many of those affected have stomach and intestinal disorders.
Idic (15) syndrome, Isodicentric 15 syndrome.
There may be some common characteristics in the diagnosis. Many children with this syndrome find it difficult to accept dental treatment and brush their teeth. Some medicines may produce side effects in the form of a dry mouth, which can increase the risk of tooth decay. Problems with sucking, eating and swallowing occur mainly during infancy. Speech, language and communication difficulties are common.