Friday, October 21, 2011

Best Pracitices in Education For Children with Angelman Syndrome


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Best Practices in Education for Students with Angelman Syndrome

Rita Molino-Sell

Walden University































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Abstract

Children with Angelman Syndrome are globally developmentally disabled creating a variety of needs to consider for cognitive assessment, placement, and instruction.  This paper offers a vision of three stages to increase the opportunities for children with Angelman Syndrome to participate in inclusion.  Best Practices in education need to be considered when creating an IEP for an individual: this includes classroom placement. 































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Best Practices in Education for Students with Angelman Syndrome

            Angelman Syndrome (AS) is a neuro-genetic disorder that creates individuals to be globally delayed.  A partial deletion or mutation in maternal chromosome 15 is the cause of AS.  AS was first described in 1965 by Harold Angelman, who noticed a group of children in his pediatric practice had flat heads, made jerky movements, had protruding tongues, and had a curious high rate of smiling, happy demeanor, and bouts of laughter.  People diagnosed with AS are often referred to as Angels due to the name of the condition and also because of their happy and smiley demeanor.

            Approximately 1/20,000 births are diagnosed with AS.  Because it is a rare and unknown condition by many medical and educational professionals, this population is often underserved in both fields.  Often AS children are misdiagnosed with autism and/or cerebral palsy.  This misdiagnosis often leads to inappropriate educational placement and instruction.  AS individuals have unique abilities and learning styles that need to be considered when assessing and teaching them.

            There are listed consensus criteria to describe and diagnose Angelman Syndrome.  It must be noted that not all Angels will have all of these traits.  It is important to remember that each angel is unique and has his/her own personality traits and learning abilities and style.

            The consensus criteria as per Williams, Beaudet, Clatyton-Smith, et al. (2005):  

·         Developmental delay, functionally severe



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  • Movement or balance disorder, usually ataxia of gait and/or tremulous movement of limbs. Movement disorder can be mild. May not appear as frank ataxia but can be forward lurching, unsteadiness, clumsiness, or quick, jerky motions
  • Behavioral uniqueness: any combination of frequent laughter/smiling; apparent happy demeanor; easily excitable personality, often with uplifted hand-flapping or waving movements; hypermotoric behavior
  • Speech impairment, none or minimal use of words; receptive and non-verbal communication skills higher than verbal ones

Frequent (more than 80%)

  • Delayed, disproportionate growth in head circumference, usually resulting in microcephaly (≤2 S.D. of normal OFC) by age 2 years. Microcephaly is more pronounced in those with 15q11.2-q13 deletions.
  • Seizures, onset usually < 3 yrs. of age. Seizure severity usually decreases with age but the seizure disorder lasts throughout adulthood.
  • Abnormal EEG, with a characteristic pattern, as mentioned in the text. The EEG abnormalities can occur in the first 2 years of life and can precede clinical features, and are often not correlated to clinical seizure events.

Associated (20 - 80%)

  • Flat occiput
  • Occipital groove
  • Protruding tongue
  • Tongue thrusting; suck/swallowing disorders
  • Feeding problems and/or truncal hypotonia during infancy
  • Prognathia
  • Wide mouth, wide-spaced teeth
  • Frequent drooling
  • Excessive chewing/mouthing behaviors
  • Strabismus
  • Hypopigmented skin, light hair and eye color (compared to family), seen only in deletion cases
  • Hyperactive lower extremity deep tendon reflexes
  • Uplifted, flexed arm position especially during ambulation
  • Wide-based gait with pronated or valgus-positioned ankles
  • Increased sensitivity to heat
  • Abnormal sleep wake cycles
  • Attraction to/fascination with water; fascination with crinkly items such as certain papers and plastics
  • Abnormal food related behaviors
  • Obesity (in the older child)

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  • Scoliosis
  •  Chronic Constipation

Upon reading this long list of traits, one might believe this population is severely mentally retarded.  Earlier reports and definitions of AS listed severe mental retardation as the first descriptor of this population (Williams, Fria, Optiz, 2005), however with an increase in awareness and in depth studies, it has been found and believed that Angels are able to learn and have a higher level of cognition and receptive skills than originally thought by professionals (Summers & Szmarti, 2009).

This population is often overlooked for inclusion opportunities due to various reasons:  inappropriate or ineffective assessments, untrained teachers, misguided belief systems regarding inclusion, limited knowledge and awareness of AS, limited funds in school budgets, lowered expectations for this population, and their various needs.

Inclusion opportunities for any special needs population is an age old discussion.  For decades arguments for both sides of inclusion or self-contained classrooms has been going on within districts and parents.  Some districts are better equipped to have successful inclusion programs. The No Child Left Behind Act (NCLB) 2001 primary purpose was to make schools and teachers accountable for how well their students are learning. The Individuals with Disabilities Education Improvement Act of 2004 (IDEA) partnered with NCLB have revised standards for academic achievement for special needs children, along with the measurement of their functional performance.



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 Parents and educators have questions about inclusion and the term Least Restrictive Environment (LRE).  Many believe that the IDEA requires schools to practice inclusion. In fact, the term "inclusion" is relatively new and is not included in the IDEA statute or regulations. The term used in IDEA is “mainstreaming”.  According to www.wrightslaw.com:

The IDEA's LRE or mainstreaming policy, school districts are required to educate students with disabilities in regular classrooms with their nondisabled peers, in the school they would attend if not disabled, to the maximum extent appropriate.

            It is often a misunderstanding that IDEA states that it is the law and a “right” to have full inclusion for a developmentally disabled child.  There are times when a self-contained classroom would be most appropriate for a given student.  However, it is imperative to acknowledge that all factors need to be considered when making the decision for a student’s Individualized Education Program (IEP) for full inclusion, partial inclusion, or a self-contained classroom.  Parent involvement is a critical aspect of the decision making as well.

            The important question to ask is; realistically, can we expect children with Angelman Syndrome to thrive in inclusion programs or are they destined for self-contained classrooms?  What are the best practices for this population in regards to assessment, instruction, and placement?

Best Practices in Education

            What does the term “Best Practices” mean?  It can be defined as “what works” in a particular environment or situation.   Grover J. Whitehurst, as assistant secretary for Educational Research and Improvement at the U.S. Department of Education in 2001, defined evidence-

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based education as “the integration of professional wisdom with the best available empirical evidence in making decisions about how to deliver instruction.”  The application of educational theory and research to make decisions for a child’s education involves more than how to deliver instruction, it also involves decision making for assessments and placement not just instruction.

            According to the State Education Resource Center (www.ctserc.org) there are nine standards to assess Best Practices:

1.       A Clear and Common Focus;  Administrators, teachers, students, and parents share and commit to clearly articulated and understood common goals based on the fundamental belief that all students can learn and improve their performance.  There is clear evidence of school practices to support this belief

2.      High Standards and Expectations:  Each teacher believes “all students can learn and I can teach them.” Staff members are dedicated to helping every student achieve challenging state and local standards.  All students are engaged in an appropriately ambitious and rigorous course of study in which the high standards of performance are clear and consistent and the conditions for learning are modified and differentiated.  This results in all students being prepared.

3.      Strong Leadership: School leadership is focused on enhancing the skills, knowledge, and motivation of the people in the organization and creating a common culture of high expectations based on the use of skills and knowledge to improve the performance of all students. Leadership fosters a collaborative atmosphere between the school and the community while establishing positive systems to improve leadership, teaching, and student performance.

4.      Supportive, Personalized Relevant Learning:  Supportive learning environments provide positive personalized relationships for all students while engaging them in rigorous and relevant learning.

5.      Parent/Community Involvement:  Parents and community members help develop, understand, and support a clear and common focus on core academic, social, and personal goals contributing to improved student performance and have a meaningful and authentic role in achieving these goals. The school community works together to actively solve problems and create win-win solutions. Mentoring and outreach programs provide for two-way learning between students and community/business members.

6.      Monitoring, Accountability, and Assessment:  Teaching and learning are continually adjusted on the basis of data collected through a variety of valid and reliable methods that indicate student progress and needs. The assessment results

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7.      are interpreted and applied appropriately to improve individual student performance and the instructional program

8.      Curriculum and Instruction:  Align curriculum with core learning expectations to improve the performance of all students. Students achieve high standards through rigorous, challenging learning. Staff delivers an aligned curriculum and implements research-based teaching and learning strategies. Students are actively involved in their learning through inquiry, in-depth learning, and performance assessments.

9.      Professional Development:  Ongoing professional development aligned with the school’s common focus and high expectations to improve the performance of all students is critical in high-performing schools. These professional development offerings are focused and informed by research and school/classroom-based assessments. Appropriate instructional support and resources are provided to implement approaches and techniques learned through professional development.

10.  Time and Structure:  Flexibly structured to maximize the use of time and accommodate the varied lives of their students, staff, and community in order to improve the performance of all students. The structure of programs extends beyond the traditional school day and year as well as beyond the school building. The program draws on the entire community’s resources to foster student achievement.



Assessment, Placement, and Instruction

            Having every aspect of development being affected from AS, it may prove to be difficult to accurately assess cognitive abilities.  AS individuals are nonverbal, visually impaired, fine motor and gross motor skills are affected and delayed, many have severe sensory processing disorders, hyperactivity, limited attention span, and many have seizure disorders along with other medical and physical issues.  Any one of these preceding traits can create difficulty and limitations in how accurately a child’s cognitive ability can be assessed.  Cooper (2010) found that in many cases when children who are nonverbal and have significant motor disabilities (such





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as Angelman Syndrome) “may need adaptations of testing materials or processes, specifically of input (presentation) and output (response) modes.”

            Mukhopadhyay & Nwaogu (2009) stated that ”Augmentative Alternative Communication has proven to be beneficial in the instruction of children who are nonverbal Augmentative and alternative communication (AAC) means any method of communication that helps an individual with severe communication disorders to compensate for activity limitation and enhances participation in various communicative interactions.”  Perhaps further research in the use of AAC for assessment purposes would be advantageous in finding and implementing best assessment practices for AS students. There is limited literature on appropriate assessment practices for this specific population.  It would be beneficial to parents, educators, and AS individuals alike if further research was done to review assessment tools and practices for this population. 

            Best practices in placement for children with AS and subsequently instruction and curriculum is a topic that needs further investigation as well.  There are many opinions in regards to inclusion vs. self-contained classrooms.   Implementing best practices in education for this population: assessment, placement, and instruction will fail to occur   if an increase in awareness and knowledge of Angelman Syndrome does not happen.  Misdiagnosis, misunderstanding, and underestimating the abilities and capabilities of a child with AS are also great contributors to the lack of inclusion opportunities for AS children.  I have a vision to improve the opportunities of inclusion.  It will take time, effort, fortitude, and several stages to attain this vision.





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Stage 1:  Increase Awareness and Knowledge

            As stated earlier, misdiagnosis is a primary contributor to the lack of inclusion opportunities for children with Angelman Syndrome.  Many medical professionals do not know of this syndrome or lack extensive knowledge of this disorder to correctly diagnose children.  Often children are misdiagnosed with autism and/or cerebral palsy (Williams, Lossie, & Driscoll, 2001).  There may be some similarities amongst these conditions; however, there are many specific identifying behaviors and traits attributed to Angelman Syndrome.  Another contributor to misdiagnosis could be that parents may be overwhelmed with all of the aspects in caring for a special needs child and not know that their child is misdiagnosed.

 The first step in achieving an increase in AS students in inclusion classrooms is to bring awareness, educate, and inform parents, medical, and educational professionals.  In order to accomplish this, I plan on providing pediatric offices with educational brochures and information regarding the criteria in diagnosing Angelman Syndrome.  The earlier a child is correctly diagnosed the quicker appropriate educational and therapeutic plans can be set into place. 

Stage 2:  Establish the Existing Belief System Towards Inclusion vs. Self-Contained Classrooms

 I will evaluate and analyze various educational trends. I will look at surrounding districts and assess what is working and not working within their inclusion classrooms. Next, I will survey and interview teachers, students, and parents to receive feedback about current teaching practices. I will also look at current belief systems from educators and parents on inclusion including any obstacles or apprehensions to pursue increasing the amount of inclusive

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classrooms.   In order to establish an existing belief system in regards to inclusion vs. self-contained classrooms, a self-administered survey can be implemented for parents and educators. A data analysis of local districts and the percentage of developmentally disabled students placed in their home schools inclusively or segregated or placed in a special school with no opportunity for inclusion.  Also a contrast and comparison amongst districts can be completed to determine satisfaction level of parents and educators with inclusion policies and practices.  Face to face interviews would also be beneficial to acquire a data base to establish current belief systems.  These surveys, interviews, and data analysis, hopefully will contribute to establishing a needs assessment of an increase in the opportunities for children with Angelman Syndrome to be included in educational settings with their non disabled peers.



Stage 3:  Educate and Inform

            Upon completion of gathering and interpreting data, sharing an opportunity with leaders, professionals, and parents to educate and inform them on the benefits inclusion and ways to implement inclusion for students with Angelman Syndrome.  Invitations to open forum discussions and/or lecture style seminars can be beneficial.  Finally, I will develop effective instruction that models and coaches teachers by implementing strategies that promotes profound learning for the diverse population in their classrooms. Support staff will be available as needed for the students with IEPs. Students who require additional services will be able to access those services within their school day and as push in therapy (when possible) and not be entirely segregated from their peers.  McCarty (2006) stated several benefits to inclusion.  “The special



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needs student is able to develop relationships with peers that are non-disabled.  The general education student also benefits from understanding people with disabilities”. 

Academic benefits are not only for the student with special needs but also for general education students.  “Academic benefits for general education students include having additional special education staff in the classroom, providing small-group, individualized instruction, and assisting in the development of academic adaptations for all students who need them” (Hines, 2001, P. 3).  Research has also shown that special-needs students in inclusion do better academically and socially than comparable students in non-inclusive classes (Irmisher, 1995).

There is research that also depicts disadvantages to inclusion.   Increase in support staff equates to increase in cost to districts. Ongoing teacher training adds to the cost as well.  Some have argued that the non-disabled students will lose learning opportunities due to an increase in the special needs students’ disruptive behavior (McCarty, 2006).   Educators and parents of children in general education worry that full inclusion will lower the standard of learning for the class and make it less of a priority than socializing (Irmsher, 1995).  

Conclusion

In order to follow Best Practices throughout the implementation of the stages to increase the opportunities of AS students for inclusion, I will follow and abide by the nine standards listed above.  There is research on inclusion for students with various developmental delays and disabilities. There is limited research on inclusion for students with Angelman Syndrome.  Leyser & Kirk (2011) recently published an article on parent’s perspectives on inclusion and their AS child’s schooling.  This study showed that parents who children who were involved in some form of inclusion had a more favorable attitude toward inclusion compared to parents who

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were mainly educated in segregated settings.   This finding reinforces the need to inform parents of children with Angelman Syndrome all of their options in regard to inclusion.   Many parents shared satisfaction with the positive relationship with teachers they perceived as caring and committed.  Yet 40% of the parents in this study were critical in regards to their relationships with the school and district administration.  Perhaps this is a red flag for leaders to be more open to improve communication and relationship status with parents of special needs children.

I am in complete agreement with Leyser & Kirk (2011) when they stated “future research should continue to examine the perspectives of parents of children with different diagnostic characteristics and educational needs regarding inclusion.”  A thorough and in depth study would benefit this population greatly.  Future research to investigate which forms of alternative assessment and instruction solicit the best responses from AS children is needed to determine appropriate classroom placement. 

Inclusion can be cost-effective if approached and implemented correctly.  Assessing the individual child’s needs and what support systems will need to be in place for the teacher and student in order for inclusion to be considered successful and beneficial to all involved.

 A child with Angelman Syndrome presents unique considerations for inclusion.  Perhaps an additional question that needs to be asked is if total inclusion, partial inclusion, or self-containment is the most appropriate for a child with AS?  More research needs to be done on the benefits of inclusion, and partial inclusion (for example part of the day in self-contained classroom, and part of the day spent in inclusion with non disabled peers) for students with Angelman Syndrome. 



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AS children are capable of learning.   They just have additional special needs that if properly assessed, can thrive in all areas of academia.   In order to step into their full potential, they need the same opportunity to access all the benefits their non disabled counterparts have in education. 

Finally, it must be recognized that each individual has his/her own unique needs, capabilities, learning styles, and disabilities that require individual attention.  Each parent with a special needs child, specifically Angelman Syndrome, needs to be informed of what their options are for their child’s education.  The best decision is a well informed decision.




















 References

Angelman, H. (1965). Puppet Children: A report of three cases. Developmental Medicine & Child Neurology, 7(6), 681-688.

Cooper, M. A. (2010). Cognitive Assessment of Nonverbal young Children Who Have Significant Motor disability:  challenges and Solutions. Physical Disabilities:  Education and Related Services, XVIII, 19-33.

Hines, R. A. (2001). Inclusion in middle schools. Urbana, IL: Eric Clearinghouse On Elementary And Early Childhood Education, University Of Illinois.

Irmsher, K. (n.d.). Inclusive Education in Practice: The Lessons of Pioneering School Districts. www.eric.ed.gov. Retrieved October 14, 2011, from www.eric.ed.gov/PDFS/ED380913.pdf

Leyser, Y., & Kirk, R. (2011). Parents' Perspectives on Inclusion and Schooling of Students with Angelman Syndrome:  Suggestions for Educators. International Journal of Special Education, 26(2), 79-91.

McCarty, K. (2006, March 11). Full Inclusion: The Benefits and Disadvantages of Inclusive Schooling. An Overview. ERIC รข€“World€™s largest digital library of education literature. Retrieved October 14, 2011, from http://www.eric.ed.gov/ERICWebPortal/search/detailmini.jsp?_nfpb=true&_&ERICExtSearch_SearchValue_0=ED496074&ERICExtSearch_SearchType_0=no&accno=E6074







Mukhopadhyay, S., & Nwaogu, P. (2009). Barriers to Teaching Non-Speaking Learners with Intellectual Disabilities and Their Impact on the Provision of Augmentative and Alternative Communication.  International Journal of Disability, Development and Education, 56(4), 349-362. Retrieved from EBSCOhost

Petersen, M. B., M.D., K. B., Hansen, L. K., & Wulff, K. (1995). Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: Estimated prevalence rate in a Danish county. American Journal of Medical Genetics, 60(3), 261-262.

Runswick-Cole, K. (2008). Between a Rock and a Hard Place:  Parents’ Attitudes to the Inclusion of Children with Special Educational Needs in Mainstream and Special schools. British Journal of Special Education, 35(3), 17-180. Retrieved from EBSCOhost.

Summers, J., & Szatmari, P. (2009). Using Discrete Trial Instruction to Teach Children with Angelman Syndrome. Focus on Autism and Other, 24(4), 216-226.

Williams, C., Beaudet, A., Wagstaff, J., Clayton-Smith, J., Knoll, J., Kyllerman, M., et al. (2006). Angelman syndrome 2005: updated consensus for diagnostic criteria. American Journal of Medical Genetics, 140(5), 413-418.

Williams, C. A., Lossie, A., & Driscoll, D. (2001). Angelman Syndrome: Mimicking Conditions and. American Journal of Medical Genetics, 101, 59-64.