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A small percentage of infants with cri-du-chat syndrome are born with serious organ defects (especially heart or kidney defects) or other life-threatening complications that can result in death.
Most fatal complications occur before the child’s first birthday.
Children with cri-du-chat who reach age 1 generally will have a normal life expectancy.
But the child will most likely have lifelong physical or developmental complications.
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Even if you don’t display symptoms, you may be a carrier if you have a family history of the syndrome.
The severity of your child’s symptoms depends on how much genetic information is missing from chromosome 5.
Some symptoms are severe while others are so minor they may go undiagnosed.
The exact reason for the chromosome 5 deletion is unknown.
In most cases, the chromosome break happens while the parent’s sperm or egg cell is still developing.