Genetic testing can confirm the diagnosis. Health professionals can diagnose Cri du Chat syndrome based on the syndrome’s distinctive cry.If you have a child with Cri du Chat syndrome, you can choose to have your own chromosomes tested if you’re thinking of having more children. Cri-du-chat syndrome usually happens by chance, but in 10-15% of cases it’s inherited.Cri-du-chat syndrome is rare and happens in around 1 in 20,000-50,000 births.Cri du Chat syndrome is a rare genetic disorder that causes health problems and intellectual disability.Because symptoms may vary from individual to individual, it is recommended that parents discuss these options with a health care professional to develop a personalized plan for therapy. While there is no specific treatment available for Cri-du-chat syndrome, early intervention is recommended in the areas of physical therapy (achieving physical and motor milestones such as sitting and standing up), communication (speech therapy, sign language instruction), behavioral modification (for hyperactivity, short attention span, aggression), and learning (special education) 2). ![]() Cri-du-chat syndrome is found in people of all ethnic backgrounds.Ĭri-du-chat syndrome usually happens by chance, but in 10-15% of cases it’s inherited. Cri-du-chat syndrome is slightly more common in girls.
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