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Angelman Syndrome
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Published on Nov 18, 2015
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PRESENTATION OUTLINE
1.
ANGELMAN SYNDROME
BY:REBEKA WAITE
2.
WHAT IS IT?
Angelman Syndrome is a genitive disordor
It is caused by mutations is the egg gametes
It was discovered in 1965, by Dr. Harry Angelman
Dr. Angelman noticed that 3 patients, all being treated
for different disorders, had similar symptoms...
3.
WHAT IS IT?
normally connected to their respected disorders. He drafted
a few theories, and named the disorder Happy
Puppet Disorder, because of the puppet-like way of
walking and excessive cheerfulness of the patients. The name
was also influxes by this painting, belived to show a child with AS.
4.
Untitled Slide
(The name of that painting is Boy with a Puppet)
The name was later changed to Angelman Syndrome
mainly because the name was thought derogatory.
5.
WHAT CAUSES IT?
Angelman Syndrome was first confused with Prader-‐‑Willi syndrome
This is because both are caused by a mutation in the 15th chromosome.
The difference is, Prader-‐‑Willi syndrome is caused by a mutation on the
Paternaly inherited chromosomes. BUT
Angleman syndrome is caused by a maternal chromosome mutation.
Photo by
rarediseaseday
6.
WHAT CAUSES IT?
Angleman syndrome is caused when the maternal chromosome 15
has something wrong with the gene UBE3A
A small percentage of people with Angelman Syndrome
have 2 parental chromosome 15
The reason the causes Angelman Syndrome is because some parts
7.
WHAT CAUSES IT?
of the brain require the use of UBE3A, which is only found
In the maternal chromosome 15.
The lack of UBE3A causes the brain to act/react
differently, in Angelman Syndrome
The mutations of UBE3A can be deletion, UPD, ID, or Gene Point mutation
8.
TYPES OF MUTATIONS
Maternal Deletion: the UBE3A is deleted.
This is the cause of about 70% of cases
Parental UPF: when there are 2 parental chromosome 15
This causes 2-3% of cases
9.
TYPES OF MUTATIONS
Inparenting defect: this means that in the egg cell, UBE3A
was not "turned on"
This causes about 3-5% of cases
Mutation: UBE3A is point mutated during meiosis
This causes 5-10% of cases
10.
SYMPTOMES
Hyperactivity, Excessive laughter and smiling
Slow mental and phisical development
Seizures, sleep disorders
Limited vocabulary
11.
CURE AND TREATMENT
There is no cure currently, but FAST is working on it.
Symptoms- such as seizures and mental developement-
can be treated by therapy (such as medicine to prevent
seizures, and speech therapy to improve communication
12.
DIAGNOSIS
When AS parents notice their child is not developing
normally, the docter usually give the child a phisical
exam, then a speech test. If both results point to AS
the child will undergo a genetics test.
This tests the levels of UBE3A in the child.
Photo by
ragesoss
13.
KARYOTYPE
OF SOMEONE WITH AS
14.
Untitled Slide
15.
OTHER INTESTING FACTS
Angelman syndrome is often shortened to AS
Most people with AS have a Vocab of 0-10 words
50% of people with AS are mis-diagnosed at the
first diagnosis because of it similarities to other
disorders and because it is a fairly recent discovery
16.
OTHER INTERESTING FACTS
Feb. 15 is International Angelman Syndrome Day
AS occurs roughly in 1/15,000 births
People with AS are typically called "Angels"
both because of the name of the disorder, and
because of their generally happy attitude
17.
RECAP
Angelman syndrome is a chromosomal, sex linked disorder
It occurs because of a random mutation on chromosome 15
There is no cure, but it is being worked on, and therapy helps
with some symptoms. Angels have a normal life span.
18.
SOURCES
William, Charles A., Sarika U. Peters, and Stephen N. Calculator. Facts About Angelman Syndrome.
7th ed. 2009. Print.
202009%203-19-10.pdf>.
.
angelman.org
. Angelman Syndrome Foundation , n.d. Web. 11 Feb 2014.
.
cureangelman.org
. Foundation for Angelman Syndrome Therapuetics, n.d. Web. 11 Feb 2014
19.
SOURCES
. "Angelman Syndrome." Genetics Home Reference. N.p., 01 010 2011. Web. 11 Feb 2014.
.
. "Angelman Syndrome." Medicine Net. Medicine Net, n.d. Web. 11 Feb 2014.
.
Hewitt, John. Angelman Syndrome: Causes, Tests, and Treatments. 2010. Print.
20.
SOURCES
Lyman, Pamela. In the Company of Angels. Mustang, Oklahoma
: Tate Publishing, 2012. Print.
. "Angelman Syndrome." National Center for Biotechnology Information. N.p., 21 01 2011.
Web. 11 Feb 2014.
.
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