Max

Boy, Born August 2009
PRC

Probable Polands Syndrome  (characterized by left nipple & pectoralis major absent, and syndactylia of 2 fingers)
dysraphism right eye, drooping mouth.

Max is very quiet but does like it when visitors interact with him. He is very interested in his surroundings, is easy to please and loves to laugh. Being tickled is one of his favorite things and he also enjoys playing with toys.

He had a genetics evaluation via photos and internet consultation in 2011, and it’s believe he could have a chromosomal deletion or duplication.  Poland syndrome/sequence is sometimes associated with Moebius syndrome (6th and 7th nerve palsy) and occasionally Goldenhar Syndrome.   It is recommended that he getting a chromosomal microarray (CMA) to rule out chromosomal abnormalities. This blood test is not available in his country, but the test could be done after adoption.

$162.90 has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!


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