Angelman Syndrome: Difference between revisions
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== Clinical Presentation == | == Clinical Presentation == | ||
* Observable Presentation | * Observable Presentation | ||
** Facial features - thin upper lip, wide spaced teeth<ref name=":0" /> | ** Facial features - thin upper lip, wide spaced teeth<ref name=":0" /> | ||
** Scoliosis (20% of children/50% adults) <ref>Angelman Syndrome Guideline Development Group. Management of Angelman Syndrome: A Clinical Guideline Version:1. University of Manchester, 2010.</ref> | ** Scoliosis (20% of children/50% adults) <ref>Angelman Syndrome Guideline Development Group. Management of Angelman Syndrome: A Clinical Guideline Version:1. University of Manchester, 2010.</ref> | ||
* Motor Presentation | * Motor Presentation<ref name=":0" /> | ||
** tremors, jerkiness, and ataxia | |||
** Loss of balance and wide-based gait | |||
* Behavioural Presentation<ref name=":0" /> | * Behavioural Presentation<ref name=":0" /> | ||
** Developmental delay is normally seen within the first year of life | ** Developmental delay is normally seen within the first year of life | ||
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** Mouthing of objects | ** Mouthing of objects | ||
** Happy demeanor with increased laughter, and often an attraction to water | ** Happy demeanor with increased laughter, and often an attraction to water | ||
* Additional Comorbidities that present<ref name=":0" /> | * Additional Comorbidities that present<ref name=":0" />: | ||
** Seizures (60% of individuals) | ** Seizures (60% of individuals) | ||
** Autism spectrum disorder (ASD), | ** Autism spectrum disorder (ASD), | ||
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*** gastroesophageal reflux | *** gastroesophageal reflux | ||
* Changes in Presentation with age | * Changes in Presentation with age<ref>Genetics Home Reference. Angelman Syndrome. <nowiki>https://ghr.nlm.nih.gov/condition/angelman-syndrome</nowiki> (accessed 2 May 2018)</ref>: | ||
** As individuals with Angelman Syndrome age they often become less excitable but continue to have intellectual disability, difficulty with speech, and seizures throughout their lives (Genetics Home Reference, 2015). | |||
== Diagnostic Procedures == | == Diagnostic Procedures == | ||
Revision as of 18:12, 4 May 2018
Description of Angelman Syndrome *note: this is a student project that is still being completed[edit | edit source]
Complex genetic disorder affecting the nervous system. It is characterized by severe learning difficulties, motor dysfunction, seizure disorder, and often a happy, sociable disposition.
Prevalence[edit | edit source]
Affects approximately 1 in 15,000 individuals[1]
Epidemiology[edit | edit source]
- Onset is usually before the age of 3 [1]
- Caused by 4 molecular mechanisms [2]
- Maternal deletions of chromosome 15q11-q13 (70-80%)
- Intragenic mutation in maternally inherited UBE3A which is found in chromosome 15q11-q13 (10-20%)
- Paternal uniparental disomy (UPD) in chromosome 15q11-q13 (3-5%)
- Imprinting defects in chromosome 15q11-q13 which change the expression of UBE3A (3-5%)
- Those with deletion have more severe disease and those with UPD and imprinting have less severe defects [1]
Clinical Presentation[edit | edit source]
- Observable Presentation
- Motor Presentation[1]
- tremors, jerkiness, and ataxia
- Loss of balance and wide-based gait
- Behavioural Presentation[1]
- Developmental delay is normally seen within the first year of life
- most patients lack speech completely but those mildly affected can speak a few words
- Severe intellectual disability
- Hyperactivity and short attention span
- Mouthing of objects
- Happy demeanor with increased laughter, and often an attraction to water
- Developmental delay is normally seen within the first year of life
- Additional Comorbidities that present[1]:
- Seizures (60% of individuals)
- Autism spectrum disorder (ASD),
- Digestive system complications
- constipation
- gastroesophageal reflux
- Changes in Presentation with age[4]:
- As individuals with Angelman Syndrome age they often become less excitable but continue to have intellectual disability, difficulty with speech, and seizures throughout their lives (Genetics Home Reference, 2015).
Diagnostic Procedures[edit | edit source]
Patients with Angelman Syndrome are often diagnosed within their first year of life. Diagnosis should be confirmed with genetic testing to determine DNA methylation [1]
Differential Diagnosis
[edit | edit source]
add text here relating to management approaches to the condition
Outcome Measures
[edit | edit source]
add text here relating to the differential diagnosis of this condition
Physiotherapy Management and Treatment
[edit | edit source]
text here
Additional Treatment[edit | edit source]
- Occupational therapy:
- Play a key role in treating fine motor skills, and self management skills to perform activities of daily living.
- Speech Language Pathology
- Play a key role in treating difficulties with both communication and swallowing.
Clinical Guidelines for Angelman Syndrome[edit | edit source]
For more detailed information on the treatment of Angelman Syndrome across several health care providers, clinical guidelines have been created by the Angelman Syndrome Guideline Development Group. Visit their document here [1].
Additional Resources[edit | edit source]
Canadian Angelman Syndrome Society:
- Visit their webpage here [2]
FAST: Foundation of Angelman Syndrome Therapeutics
- Visit their webpage here [3]
- Below is a video about Angelman Syndrome created by FAST Australia
References[edit | edit source]
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 Margolis SS, Sell GL, Zbinden MA, Bird LM. Angelman syndrome. Neurotherapeutics. 2015 Jul 1;12(3):641-50.
- ↑ Kishino T, Lalande M, Wagstaff J. UBE3A/E6-AP mutations cause Angelman syndrome. Nature genetics. 1997 Jan;15(1):70.
- ↑ Angelman Syndrome Guideline Development Group. Management of Angelman Syndrome: A Clinical Guideline Version:1. University of Manchester, 2010.
- ↑ Genetics Home Reference. Angelman Syndrome. https://ghr.nlm.nih.gov/condition/angelman-syndrome (accessed 2 May 2018)
