Information on Infantile Spasms
Infantile spasms also called West syndrome.
Infantile spasms are an uncommon to rare and grave form of epilepsy in infants. About 60% of the affected infants have some brain disorder or brain injury before the seizures begin, but the others have had no apparent injury and have been developing normally. Infantile spasm (IS) is a specific type of seizure seen in an epilepsy syndrome of infancy. The syndrome is age-related, generally occurring between the third and the twelfth month, generally manifesting around the fifth month. The syndrome is often caused by an organic brain dysfunction whose origins may be prenatal, perinatal or postnatal.
Complete Information on Angelman syndrome with Treatment and Prevention
The Angelman synthesis symptom is affects the nervous system the complex gene to be chaotic. AS is a classic example of genetic imprinting caused by deletion or inactivation of critical genes on the maternally inherited chromosome.
This gene is the existence in the mother and the father chromosome, but differently in methylation style. Other causes include uniparental disomy, translocation, or single gene mutation in that region. However, in the region of the chromosome that is critical for Angelman syndrome, the maternal and paternal contribution express certain genes very differently. Children with Angelman syndrome usually present with delay in reaching their developmental milestones and often do not learn to sit until around one year of age. Although Angelman Syndrome is usually not recognized at birth or in infancy since the developmental problems are nonspecific during this time.
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