ANGELMAN SYNDROME(AS) is a rare genetic neuro-developmental disorder characterized by severe developmental delay, sleep disorders, jerky movements and frequent laughter.It was first discovered in the year 1965 by a British Pediatrician, Dr. Harry Angelman.
The syndrome is caused by an abnormality in a region of chromosome 15 and it’s usually not recognized at birth.AS is typically diagnosed between the ages of 3 and 7.
The main characteristics of this syndrome are delayed motor skills, minimal or absence of speech, developmental delay, ataxia (shaky and unsteady movements), seizures, constant happy behavior that includes frequent laughing, smiling and excitability.
The exact prevalence of AS is unknown, but it is estimated that it affects 1 in 12000-20000 people.
“ We are a family ” A family whose reason of happiness is an angel. We at this foundation wish to spread the smile in the families around the world living with such angel kids.
With the help of the foundation we wish to connect to all the families living with Angelman Syndrome nationally as well as internationally so that we can create a better world for the Angels.
The ICNC2018 is being hosted by the Child Neurology Group, Mumbai with AOCN/ICNA from 15th to 18th November 2018 at the Grand Hyatt, Santacruz, Mumbai. This will be attended by doctors / paramedical professionals with interest in child neurology from India/ Asia and indeed from across the world (approx.1000 delegates have registered.).
A glimpse of our article on Newshook! Spread the word! & let India know about *Angelman Syndrome!*