West syndrome (infantile spasms)
Last checked 25/06/2008
Epilepsy Action is indebted to Dr Richard Appleton, a Consultant Paediatric Neurologist who specialises in children’s epilepsy, and to Dr Rachel Kneen, Consultant Paediatric Neurologist and Dr Stewart Macleod, Specialist Registrar in paediatric neurology, at Alder Hey at Alder Hey Children’s Hospital, Liverpool, who have kindly prepared the information on this page.
Infantile spasms are a type of epilepsy with a characteristic age of onset (typical age when seizures start), pattern of seizures and electroencephalogram (EEG). This means that it is an ‘electroclinical epileptic syndrome’.
They can also be called ‘salaam spasms’, because the appearance of the seizures is like a bowing forwards or backwards movement, or ‘West syndrome’ after Dr West who first described the condition in his own four month old son in 1841.
This type of epilepsy occurs in about one in 3000 children. Every year in the UK about 350-400 children will develop West syndrome
Symptoms
In nine out of 10 children with the condition, infantile spasms occur in the first year of life, typically between three and eight months old. Often, to begin with, the attacks are brief, infrequent and not typical of the syndrome, so it is quite common for the diagnosis to be made late. Frequently, because of the pattern of attacks and the cry that a child gives during or after an attack, they are initially thought to be colic.
The typical pattern is of a sudden flexion (bending forward) in a tonic (stiffening) fashion of the body, arms and legs. Sometimes, however, the episodes are extensor (arching). Usually, they are symmetrical (affecting both sides equally) but sometimes one side is affected more than the other.
Typically, each episode lasts just one or two seconds, there is then a pause for a few seconds followed by a further spasm. While single spasms may happen, infantile spasms usually happen in ‘runs’ or ‘clusters’ of several in a row.
It is common for babies who have infantile spasms to become irritable and for their development to slow up or even to go backwards until the spasms are controlled. These infants can also behave as if they cannot see, but this improves once the spasms are controlled and the EEG has improved.
Diagnosis
The diagnosis of infantile spasms is made by a combination of the typical features with a typical EEG. The EEG shows a very disorganised pattern termed ‘hypsarrhythmia’. The EEG is always abnormal in children with West syndrome but sometimes this abnormality is seen only during sleep.
Infantile spasms, like many other ‘electroclinical syndromes’, have lots of different causes. A particular cause will be found in seven or eight children out of every 10 children with West syndrome.
Most children with infantile spasms will need a number of tests (EEG, brain scans, blood tests, urine tests and, sometimes, spinal fluid and other tests) in order to try to identify the underlying cause.
Treatment
The main treatments used are steroids or vigabatrin (Sabril), Nitrazepam and sodium valproate (Epilim), may also be used. The type of steroids used are prednisolone or tetracosactide. Steroids must be used carefully as this treatment may cause some unpleasant side effects.
Prognosis (outlook)
In some children, infantile spasms respond easily to treatment, whereas in others they remain very resistant. Most children unfortunately go on to have other kinds of seizures in later childhood including an epilepsy syndrome called the Lennox-Gastaut syndrome. Most children also have learning difficulties. The prognosis for infantile spasms in both these respects is largely dependent on the underlying cause of the condition.
Support organisations
West Syndrome Support Group, c/o Contact a Family, 209-211 City Road, London, EC1V 1JN, telephone 0808 808 3555, www.cafamily.org.uk
Contact a Family, 209-211 City Road, London, EC1V 1JN, telephone 0808 808 3555, www.cafamily.org.uk
14 March 2007
Epilepsy advice and information
- What is epilepsy?
- Children
- Depression
- Disability Discrimination Act (UK)
- Driving
- Education
- Employment
- Epilepsy in later life
- Getting a diagnosis
- Health care and welfare benefits
- Inheritance
- Learning disabilities
- Me and my dad
- Memory
- Men and epilepsy
- Mobile phones and epilepsy
- Osteoporosis, osteomalacia and epilepsy
- Photosensitive epilepsy
- Relationships and epilepsy
- Safety
- Seizures
- Sports and leisure
- Stress and epilepsy
- Sudden Unexpected Death in Epilepsy (SUDEP)
- Syndromes
- Aicardi syndrome
- Angelman syndrome
- Benign epilepsy of childhood with occipital paroxysms (BECOP)
- Benign myoclonic epilepsy in infancy
- Benign partial epilepsy in infancy
- Benign rolandic epilepsy
- Childhood absence epilepsy (CAE)
- Early myoclonic encephalopathy
- Electrical status epilepticus during slow-wave sleep (ESESS)
- Epilepsy with myoclonic absences
- Gelastic Epilepsy
- Generalised epilepsy with febrile seizure plus (GEFS+)
- Juvenile myoclonic epilepsy (JME)
- Landau Kleffner Syndrome
- Lennox-Gastaut Syndrome
- Migrating partial epilepsy in infancy
- Myoclonic astatic epilepsy (Doose syndrome)
- Ohtahara Syndrome
- Panayiotopoulos syndrome
- Pyridoxine dependency
- Ramsay Hunt syndrome
- Rasmussen syndrome
- Rett syndrome
- Ring chromosome 20 syndrome
- Severe myoclonic epilepsy in infancy (SMEI)
- Sturge-Weber syndrome
- West syndrome (infantile spasms)
- Travel abroad
- Treatment
- Women and epilepsy
- Young people and epilepsy
- Epilepsy Action Information Reviewers (EAIRs)
- Technical editing/writing and copyright
Epilepsy Helpline
- UK freephone 0808 800 5050
- International +44 113 210 8850
- Email: helpline@epilepsy.org.uk
- Txt msg: 07797 805 390 info





