Cri du chat syndrome is a rare genetic disorder caused by a missing part of chromosome 5, affecting an estimated 1 in 20,000 to 50,000 live births. It is usually not inherited from parents and more commonly found in females. While the condition cannot be cured, symptoms such as feeding issues and speech delays can be treated through early therapy. Parents are also advised to seek counseling.
9. The condition affects an estimated 1 in 20,000 to 50,000 live
births
Found in people of all ethnic backgrounds
More common in females
10. They are to get early speech
therapy
May need a tube for feeding
Symptoms can be treated but the
disease is not treatable or curable
Skull x-ray may reveal an
abnormal angle to the base of the
skull
Parents usually get counseling
11. Department of
March of Dimes Human Genetics
The Arc— Cri Du Chat
National Syndrome
Organization on Support Group
Mental MUMS—
Retardation Mothers United
Chromosome for Moral
Disorder Outreach Support Inc
Inc. Let Them Hear
5p-Society Foundation