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AngelmanSyndrome news

Penn Orphan Disease Center Partners with FAST for Angelman Syndrome Research


Rare Disease Report - Feb 15, 2017
The Foundation for Angelman Syndrome Therapeutics (FAST) is a Section 501(c)(3) nonprofit organization singularly focused on funding research that holds the greatest promise of treating Angelman syndrome. Paula Evans, the mother of a young girl with ...
 

Lion Clubs help make a difference in Cody's life


Orange Leader - Mar 15, 2017
Cody Dunaway is a gregarious young man who was diagnosed with Angelman Syndrome at an early age. Angelman Syndrome is a rare, genetic and neurological disorder that causes severe developmental delays and learning disabilities; absence or near ...
 

Rugby union player Curtis Rona joins crusade to find cure for Angelman Syndrome


dailytelegraph.com.au - Mar 9, 2017
The 24-year-old switched codes from rugby league to union — and also decided to take on a new role as ambassador for rare, genetic condition Angelman Syndrome (AS). Rona — who played league for the Canterbury-Bankstown Bulldogs — has joined the ...
 

Angelman Syndrome - premium items on eBay

Angelman Syndrome by Bernard Dan Paperback Book (English)


 

Old and New Entities with Rett or Angelman Syndrome-Like Intellectual Disability


 

Angelman Syndrome - A Medical Dictionary, Bibliography, and Annotated Research G


 

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Angelman Syndrome books

An Angel Among Us


by: Lee Springgate
This is the story of one family's 35 year experience with a profound developmental disability. This extraordinary journey has changed their view of the world, rearranged priorities and transformed their lives. Scott has Angelman Syndrome, a genetic aberration of the 15th chromosome. He has never spoken a single word in his life and virtually all aspects of daily living are dramatically impacted by his condition. While his cognitive and physical challenges are immense, there resides within this incomparable young man a God given capacity to love and be loved.
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Angelman Syndrome: Causes, Tests, and Treatments


by: John Hewitt M.A.
Angelman syndrome is a complex genetic disorder that was first described in 1965 by the English physician Dr. Harry Angelman. At the time, three children who presented a variety of disabilities were admitted to his center. Although at first sight it looked like they were suffering from different disorders, Dr. Angelman felt that there was a common cause for their conditions. He was right. The condition--caused by a chromosomal abnormality--Angelman syndrome is typically diagnosed between the ages of three and seven, and in some cases, it is misdiagnosed for other conditions.
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Practical Rare Syndrome Manual


by: Dawn Lucan
Your child was recently diagnosed with a rare syndrome. You begin to wonder how you can help your child and what resources are available. Dawn Lucan is an educator with eighteen years of experience will share her knowledge and website resources with you.
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Angelman Syndrome


by: Bernard Dan
Clinics in Developmental Medicine No. 177

This book provides a comprehensive review of clinical and genetic issues, natural history, possible pathophysiological pathways, specific clinical problems (motor impairment, behaviour, learning difficulties, communication, sleep, epilepsy), clinical neurophysiology, neuropathology, rehabilitation and basic research in the field of Angelman syndrome. This condition is a neurogenetic disorder characterised by developmental delay, absence of speech, motor impairment, epilepsy and a peculiar behavioural phenotype.
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Angelman Syndrome videos

What does Angelman Syndrome look like?


Angelman Syndrome (AS) is a rare condition with different genotypes and varying degrees of severity affecting approximately 1:15000 births. Around 490000 ...
 

Jacob's Story, Angelman Syndrome


Young Jacob suffers from a rare disease that affects 1 in 20000 children. Studio 10 | 8:30am on TEN.
 

A Story about Angelman Syndrome


Angelman Syndrome is a rare genetic condition. You can read the clinical characteristics and what individuals and their families may go through, however it is ...
 

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Bio project on Angelman Syndrome!
 

4 siblings with Angelman Syndrome