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Owen 3G

egxb-3
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.

Owen’s grant of $4263.25 was gifted to Victor in Asia.  

 

***This child is in a country that is currently not accepting new commitments. We can no longer accept grant donations or inquiries for this child, but we have not given up on any of these children and encourage all of our Prayer Warriors to continue their efforts! When and if this country program re-opens for adoptions, we will relist this child and begin seeking an adoptive family immediately.***

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