Now I understand better: very similar to DiGeorge syndrome, phenotype
is different, therefore diagnosis remains clinical but a mutation in
CHD7 is found in 71 percent of patients fulfilling the criteria for
CHARGE.
Yes, it's highly advisable that parents take direct care of their
children when having this recently described / discovered suffering. I
have my own opinion on why this should be so.
Thank you, Ian.
Fernando.
2009/12/14 SwissPace <ian@xxxxxxxxxxxxxxxx>:
> Cai has charge syndrome,
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