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AngelmanSyndrome news

Cavion Raises $26.1M in Series A Funding


FinSMEs (blog) - Jan 9, 2017
... a common pathophysiology of neurological diseases such as Essential Tremor, Parkinson's Disease, Neuropathic Pain, and Epilepsy as well as orphan neuro-developmental and genetic disorders such as Angelman Syndrome and Dravet Syndrome.
 

Star Wars charity film success delights Nuneaton family


Nuneaton News - Jan 5, 2017
Ella is the niece of Gareth Edwards and he is the patron of ASSERT, the Angelman Syndrome Support Education and Research Trust, of which his sister and Ella's mum, Lisa, is a trustee. The film, which was made on set of the smash-hit Rogue One and ...
 

Mother with disabled son faces homelessness this New Year after pre-Christmas eviction


Express.co.uk - Jan 1, 2017
The council for Rhostryfan, north Wales, is unable to find accommodation because of a lack of disabled-friendly houses suitable for James, who suffers Angelman Syndrome, a severe developmental disability. Now leading charities are calling for an ...
 

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

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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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


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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Prader-Willi Syndrome: and Other Chromosome 15q Deletion Disorders


Although Prader-Willi syndrome was first described 35 years ago, it was following detection of an interstitial chromosome 15q deletion in some affected patients ten years ago that it became a major focus of multidisciplinary scientific interest. This interest was compounded by the later determination that some patients with a clinically distinct disorder, Angelman syndrome, apparently also had the same chromosome 15q deletion. Subsequently, molecular genetic studies showed that some cytogenetically normal patients with both disorders have uniparental disomy, maternal in Prader-Willi syndrome and paternal in Angelman syndrome.
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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 ...
 

4 siblings with Angelman Syndrome


 

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Bio project on Angelman Syndrome!