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Segawa syndrome, also called dopa-responsive dystonia, is an inherited disease that can cause physical rigidity and developmental delay. There are two forms: mild and severe.
In the mild form, symptoms typically begin in childhood. Children develop jerky movements that quickly progress to physical rigidity. These children show spastic movements, and make very little voluntary movement. If untreated, children with Segawa syndrome may have expressionless faces, drooping eyelids, tongue tremors, and drooling problems. They will show both mental and physical developmental delays. Some children with Segawa syndrome show a “diurnal” pattern, meaning their symptoms are more or less severe on alternate days. With early treatment, children with Segawa syndrome can avoid many or all of the disease’s symptoms.
The severe form of the disease will appear in infancy, usually before six months of age. Affected infants have delayed motor skills, weakness in the chest and abdomen, rigidity in the arms and legs, and problems with movement. These children will eventually have learning disabilities, problems with speech, and behavioral/psychological problems. In addition, some people with the disease have problems with their autonomic nervous system, which regulates unconscious functions such as body temperature regulation, digestion, blood sugar level, and blood pressure. Treatment of the severe form of the disease is often less successful.
Segawa syndrome is caused by a deficiency in an enzyme called tyrosine hydroxylase. Without it, the amino acid tyrosine cannot properly be converted to dopamine, a key neurotransmitter in the brain. Dopamine is important for many functions, including muscle control and cognition.
Note that there is another type of Segawa syndrome with a different genetic basis that is not addressed here.
The prevalence of Segawa syndrome is unknown, and only a small number of cases have been diagnosed globally. Cases have been reported in Japan and in the Netherlands.
Individuals with the mild form of Segawa syndrome respond well to treatment with supplements of L-dopa and carbidopa. If taken before symptoms appear, the symptoms may be avoided completely. If symptoms have already begun, children with the disease often respond extremely well to the medication, returning to normal very quickly. If the disease has gone untreated for some time, certain symptoms may remain, including an irregular gait and other mild movement and speech difficulties.
Treatment with L-dopa and carbidopa supplements has been less beneficial for individuals with severe Segawa syndrome, but this treatment may improve motor skills over time.
If symptoms have gone untreated, physical, occupational, and/or speech therapists may prove helpful.
With early and consistent treatment, the prognosis for a person with mild Segawa syndrome is good. Many symptoms can be reversed with treatment. If treatment is not begun early and/or the course of the disease is severe, the person may be shorter than they would otherwise have been and may have an irregular walk and/or learning disabilities.
An organization that helps individuals with dystonia and their families cope with the disease. It provides educational materials about the conditions that cause dystonia, as well as links to treatment and support groups.
One East Wacker Drive, Suite 2810
Chicago, IL 60601
Phone: (312) 755-0198
Secondary Phone: (800) 377-3978
A description of dopa-responsive dystonias including Segawa syndrome, written in fairly scientific language. It is, however, an accurate and thorough description of the condition.
A volunteer non-profit organization aimed at helping children and families who are affected by diseases such as Segawa syndrome, supporting the identification of new diseases of this kind, and finding better treatments for diseases that are already known.