Jox
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OH and stepson both have the missing part of the chromosome. Missing it can affect a person in different ways. It looks as tho OH isn't affected by it but stepson is. Stepson is autistic with learning difficulties. He goes to a special school and will never live independently. He able, under instruction, to get dressed, brush his teeth etc but can't make his own drink, sandwich, has no sense of danger, can't be left alone etc his autism is quite bad but from reading possible effects he isn't too bad if that makes sense?
The 2p16.3 is the chromosome deletion. So they r missing a part of chromosome number 2. The deletion is labelled NRXN1. If u google them ull probably get more sense than from me.
Basically, even if she has the deletion she may not be affected by it. She has 50/50 chance that OH has passed the deletion on to her xx
The 2p16.3 is the chromosome deletion. So they r missing a part of chromosome number 2. The deletion is labelled NRXN1. If u google them ull probably get more sense than from me.
Basically, even if she has the deletion she may not be affected by it. She has 50/50 chance that OH has passed the deletion on to her xx