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1p36 Deletion Support & Awareness


 1p36 Deletion Support & Awareness (1p36 DSA) is a non profit

501 (c) 3 organization that is composed primarily of parents and

caregivers of individuals affected with 1p36 Deletion Syndrome. 

Our Mission is to help individuals affected by chromosome
1p36 abnormalities overcome the obstacles they face to be
able to lead healthy, happy and productive lives.
 

 


 New on 1p36DSA.org
> 1p36 DSA 501 (c) 3 status
 
 
 
 
 In the News
 > Senator Mikulski's Statement on Introduction of Rosa's Law
 > 2009 State Ranking of Medicaid
 > H1N1 Information from the CDC 
 > Stem Cell Research
 > 1p36 Deletion Syndrome and Obesity Article
 
 
 
 Upcoming Events 
 > Feb 28th, 2010 - Rare Disease Day 
 > 2010 1p36 DSA 2010 Conference
 
 
 
 
 


What is 1p36 Deletion Syndrome?

 

1p36 Deletion Syndrome is a chromosome disorder that is characterized by moderate to severe intellectual disability, delayed growth, limited speech ability and distinct facial features. It is estimated that 1p36 Deletion Syndrome occurs in one in every 5,000 to 10,000 births though many individuals still go undiagnosed.

Typically, humans have 23 pairs of chromosomes (46 chromosomes) in a cell. 22 pairs of chromosomes are numbered 1-22 and a pair of sex chromosomes are X and Y. Each pair of chromosomes has a short arm "p" and long arm "q". 1p36 Deletion Syndrome occurs when an individual is missing (deletion) the most distal light band of the short "p" arm of chromosome 1. 1p36 Deletion Syndrome is the most common chromosome deletion.
 
1p36 Deletion Syndrome can be referred to as chromosome 1p36 deletion syndrome, distal monosomy 1p36, monosomy 1p36 syndrome, monosomy 1p36 or monosomy 1p36 deletion syndrome. To learn more about 1p36 Deletion Syndrome
CLICK HERE.
Genetics

 

New 1p36 Diagnosis?

 

Learn the basics about Genetics and chromosomes.

 

 

> READ MORE

Making a Difference

 

Making a Difference

 

Learn how parents of children with 1p36 are fundraiser for 1p36 DSA .


> READ MORE

 

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   1p36 Deletion Support

   & Awareness, click the

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