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After the diagnosis the parent will most likely see a genetic counselor.
Depending on the counselor’s experience, he/she may or may not give accurate information. Individuals with this syndrome will range from mild to severe in developmental delays. The location and type of deletion (“de novo,” mosaic, unbalanced translocation), early intervention and various therapies, and the natural variation among people all play a key role in your loved ones development.
Parents, therapists, and educators should all work together in the overall education of the child and create sustainable goals.
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A small number of children are born with serious organ defects and other life threatening medical conditions, although most individuals with 5p- can anticipate a normal life expectancy.
Both children and adults with this syndrome are usually friendly and happy, and enjoy social interaction.
Individuals with this syndrome will have his or her own timeline meeting developmental milestones.
It will be hard not to compare the child with Cri du Chat Syndrome with other “normal” children his or her age.