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Angelman syndrome (AS) is a neuro-genetic disorder characterized by intellectual and developmental delay, sleep disturbance, seizures, jerky movements especially hand-flapping, frequent laughter or smiling, and usually a happy demeanour.
Treatment
There is currently no cure available. The epilepsy can be controlled by the use of one or more types of anticonvulsant medications. However, there are difficulties in ascertaining the levels and types of anticonvulsant medications needed to establish control, because AS is usually associated with having multiple varieties of seizures, rather than just the one as is normal cases of epilepsy. Many families use melatonin to promote sleep in a condition which often affects sleep patterns. Many individuals with Angelman Syndrome sleep for a maximum of 5 hours at any one time. Mild laxatives are also used frequently to encourage regular bowel movements and early intervention with physiotherapy is important to encourage joint mobility and prevent stiffening of the joints.
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∙ 13y ago
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Is Angelman syndrome the same as Down syndrome?
Angelman syndrome is a genetic disorder, as is Down syndrome. But they are not the same. Angelman Syndrome involves a deletion of Chromosome 15, whereas people with Down syndrome have an extra copy of Chromosome 21.
What percentage of babies is born with Angelman syndrome?
Approximately 1 in 15,000 - 20,000 babies is born with Angelman syndrome, making it a rare genetic disorder.
What is Angelman's Syndrome's scientific name?
Angelman syndrome's scientific name is "AS," or "Angelman syndrome." It is a genetic disorder characterized by developmental delays, speech impairments, and unique behaviors. It is caused by a loss of function in a specific gene located on chromosome 15.
Which race has a higher chance of getting Angelman Syndrome?
this disorder does not discriminate against anyone
Is angelman syndrome autosomal?
"Autosomal" means the syndrome or disorder of interest is pertaining to a chromosome that is not a sex chromosome, either X or Y. Angelman and Prader-Willi Syndrome are both caused by a deletion (or disruption of a gene) on chromosome 15, which is an autosomal chromosome and not a sex chromosome. Therefore, yes, Angelman syndrome is considered an autosomal syndrome.
Who identified Angelman syndrome?
in 1965 Harry Angelman
What is Angelmen syndrome?
Angelman syndrome (AS) is a neuro-genetic disorder that happens once in 15,000 live births. Characteristics of the disorder include developmental delay, lack of speech, seizures, and walking and balance disorders.
Do black people have angelman syndrome?
Yes. All races and both males and females get Angelman Syndrome.
Life expectancy of angelman syndrome?
People with Angelman Syndrome often live the average life expectancy of their gender.
Is angelman syndrome a recessive or a dominant?
It is recessive
Angelman syndrome effects gender and ethnicity?
no
Is there any cure for of a genetic disease called Angelman's syndrome?
Angelman's syndrome is a genetic disorder caused by deletion on genes on chromosome 15 contributed by the mother to child, once you are born with it, the faulty gene has already done the damage. There is no cure for it. Note: If their deletion of the same gene on chromosome 15 contributed by the father, it results in Prader Willi syndrome.
