Today I would like you to meet someone who's picture has been implanted in my mind since I first saw him on the RR website -
Owen:
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His picture from 2007 or 2008 when he first got listed |
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His picture from May 2009 |
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His picture from May 2010 - the photo that drew me to him |
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His recent picture from (May?) 2011 |
Boy, Born December 2007
This darling little boy is waiting for his forever family, and we believe his condition to be one called
Saethre-Chotzen Syndrome. Also known as Acrocephalosyndyldactyly Type Chotzen or Saethre-Chotzen Syndrome. Chotzen Syndrome is a dominant genetic condition. They have a tower-shaped skull (acrocephaly), fused fingers and/or toes (syndactyly), asymmetric face, widely spaced eyes, droopy eyelid (ptosis), strabismus (crossed or "wall-eyes"), beak-like nose, small upper jaw, and jutting out lower jaw (prognathism). Some plates in their skull close early. This is called craniosynostosis. Often people with Chotzen Syndrome are mildly hard of hearing. Sometimes they're unusually short. Occasionally the closing of the plates in their skull can compress their brain and slow their development. Sometimes boys with Chotzen Syndrome have undescended testicles.
This little boy has touched my heart. I would love to adopt him but I have to convince my husband first! I hope he finds a home soon. This is a very treatable condition!
ReplyDeleteI will keep this sweet boy in my prayers.
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