West syndrome is a severe form of epilepsy most common in infancy. It is characterized by infantile spasms, hypsarrhythmia, and mental deficiency. With this said, a diagnosis of West syndrome can still be made should 1 of the 3 symptoms be absent.
The infantile spasms that result are one of three types:
- Flexor spasms resemble a brief, self-hugging motion and involve flexion of the neck, trunk, and limbs.
- Extensor spasms involve the extension of the neck, trunk, and limbs.
- Mixed flexor-extensor spasms are the most common type and involve combinations of the neck, trunk, limb flexion, and extension.
The most widely-used techniques to diagnose West syndrome include:
An EEG study uses electrodes placed on the scalp to record the brain's electrical activity. The detection of hypsarrhythmia, especially during sleep, can indicate that a patient has infantile spasms. Hypsarrhythmia is a brain wave pattern seen when seizures are not occurring and are indicated by chaotic, high-voltage spikes on an EEG. This pattern is present in wakefulness but is enhanced during sleep. Therefore, an EEG study should ideally include recordings taken during wakefulness and sleep to confirm a West syndrome diagnosis.
In some cases, simultaneous video and EEG recording (“Video-EEG”) can be used to verify particular brain-wave patterns during infantile spasms and document the patterns between the spasms.
Approximately 70-80% of patients with West syndrome present with abnormal findings on neuroimaging studies; these aim to identify West syndrome's underlying causes. It is important that neuroimaging is done before the start of specific therapies- particularly ACTH or steroid therapy- associated with the possible appearance of brain atrophy as therapy progresses.
A computed tomography (CT) scan uses X-rays to generate computerized images of cross-sections of the brain; the detail from these allows the development of the brain to be studied. On the other hand, Magnetic Resonance Imaging (MRI) scans produce detailed images of cross-sections or slices of the brain using the magnetic properties of particular atoms present in the brain.
Both imaging techniques can detect an underlying brain infection or structural abnormalities associated with the syndrome in children. Of the two, the MRI scan is much more sensitive and likely to discover the brain's abnormality. In fact, an MRI scan can show many neurologic abnormalities (such as developmental brain abnormalities) and evidence of brain injury incidents (such as those resulting from trauma, lack of oxygen, or infection).
These may be necessary to determine if there is a metabolic or genetic disease responsible for a case of West syndrome. In fact, more than 50 genetic or metabolic diseases have already been associated with the syndrome. Blood, urine, or cerebrospinal sample may be taken if family history or examination indicates the possibility of a metabolic or genetic disorder. For example, a diagnosis of nonketotic hyperglycemia requires a lumbar puncture to test for glycine.
Molecular genetic testing is also available and is already used to test for tuberous sclerosis complex (associated with symptomatic West syndrome) and mutations in genes ARX and CDKL5 (associated with X-linked West syndrome).
It is not uncommon for a diagnosis of West syndrome to be delayed, and this may occur due to many reasons:
- The EEG study does not show hypsarrythmia
- The child is considered too old to likely suffer from the disorder
- The spasms appear atypical; they may change between different seizure types or might occur singly rather than in the characteristic cluster.
- All West Syndrome Content
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Last Updated: Jan 21, 2021
Dr. Ananya Mandal
Dr. Ananya Mandal is a doctor by profession, lecturer by vocation and a medical writer by passion. She specialized in Clinical Pharmacology after her bachelor's (MBBS). For her, health communication is not just writing complicated reviews for professionals but making medical knowledge understandable and available to the general public as well.
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