English to Croatian Medical Medical (general)

Radi se o mogućnostima za prenošenje genetskih poremećaja na potomstvo koji su odgovorni za nastanak centralnog hipoventilacionog sindroma.

If an individual with the PHOX2B mutation has children, they have a 50% chance of passing on the affected gene. If carrying the gene, an individual will be affected to some extent or other, ie there is no silent carrier status. So we are now newly recognising some adults with the condition, in whom it was never suspected earlier in life.