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by Administrator last modified Sep 20, 2008 06:52 PM

What is to come now that MyDaughtersDNA.org is live! http://youtube.com/watch?v=4WOaQhjWmRU A one hour tech talk at Google on the story of My Daughter's DNA http://www.economist.com/science/PrinterFriendly.cfm?story_id=9679893 http://blogs.nature.com/wp/nascent/2007/08/post_1.html http://www.nature.com/nature/journal/v449/n7164/index.html http://www.mercurynews.com/ci_10513381?nclick_check=1

This site will always be a work in progress, in perpetual beta.  As such we are adding topics or interest and articles each week. These are primarily intended to aid the new users of the site. 

 

Over the next few months we will add some great features and functions that will help patients and physicians manage genetic health issues.  These include an interactive method to identify affected systems and related syndromes, a means to explore and annotate a graph of genes and presentations, the means to identify experts for a given disease, and an easy-to-use family tree.  Please be patient -- all of these will take time to release because we are relying on volunteers to  do the coding.  But we will get there. In the meantime, if you want to make contributions or have suggestions for features please contact us via the contact feature.

 

 

My son Alex's teeth

My son Alex's teeth

by diana allen — Sep 05, 2008 08:42 PM

This is a poor picture as it is hard to take a picture of Alex's mouth as he only has a tiny mouth that dosn't open very wide

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My son Alex's teeth

My son Alex's teeth

by diana allen — Sep 05, 2008 08:36 PM

This is a poor picture as it is hard to take a picture of Alex's mouth as he only has a tiny mouth that dosn't open very wide

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My son Alex's feet

My son Alex's feet

by diana allen — Sep 05, 2008 08:35 PM

Alex has strong acrogeria of the extremities. The hands and feet and on his arms and legs

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I am Diana, Alex's mother

I am Diana, Alex's mother

by diana allen — Sep 05, 2008 08:36 PM

I am suppose to have Ehlers-Danlos IV syndrome. I do belive i might even though my tests did not show i had the condition. My Dr's think i have as they say i look like i have it

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My son Alex

My son Alex

by diana allen — Sep 05, 2008 08:36 PM

Alex just wanted me to put up a photo of him smiling. As he did not like his other pictures

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My son Alex's face

My son Alex's face

by diana allen — Sep 05, 2008 08:36 PM

Alex has a cleft lip and a bilateral cleft pallet and a split uvula and also wide set eye's

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My son Alex's hands

My son Alex's hands

by diana allen — Sep 05, 2008 08:36 PM

This is not the best picture but his hand are very thin and look the same as his feet

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My son Alex

My son Alex

by diana allen — Sep 05, 2008 08:35 PM

Here is another picture of Alex's legs

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My son Alex

My son Alex

by diana allen — Sep 05, 2008 08:35 PM

I am trying to put up pictures of my son. So everybody can see him and maybe someone might know what Alex may have.

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My daughter

by stefan petkov — Feb 14, 2008 02:29 PM

 

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Our son Raphael : case, and search for a relevant medical team

by Jean Constant — Sep 21, 2009 11:51 AM

Boy aged 4 1/2 years, unknown peripheral neuropathy, hypotonia.

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Dev. Delay, mild facial dysmorphisms, large tongue

Dev. Delay, mild facial dysmorphisms, large tongue

by Sara B — Jan 13, 2010 06:15 PM

Updated: Description of my 2 yr. old daughter's symptoms

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My son Gage

by Susan Sifford — Aug 16, 2009 12:19 AM

A summary of my son's medical history, including physical characteristics and normal test results.

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Muscular Dystrophy by elimination - not sure

by Mohan Sundaram — Feb 01, 2009 10:05 PM

Diagnosed with a condition, alternatives explored and Muscular Dystrophy diagnosed though not explicitly

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my story

by Lauren Moynihan — Jan 27, 2009 07:50 PM

maybe someone out there knows what this is

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My Daughter Bethany

Posted by Esther Bautista at Jan 26, 2009 05:27 PM
www.mysnugly.com I found out about this site from an internet friend who read about it in wired magazine. You can read about my child and her unique characteristics at my website.

My daughter Simra

Posted by Anil Kheraj at Aug 18, 2009 07:00 PM
Please see www.angelsimra.org. My angel Simra had an undiagnosed genetic condition. She lived for a little less than a year. Her neurological condition could not be diagnosed. She passed away due to respiratory distress after contracting RSV. We miss her and do not have answers to her genetic condition.