We nonetheless believe that reporting even sporadic cases of proliferative disorders in Cd C patients may increase our knowledge as to the natural history of the disease.
Cri du Chat syndrome (Cd C) is a chromosomal abnormality (deletion of short arm of chromosome 5) associated with intellectual disability and typical anatomical abnormalities.
Research up to now focuses on the management of the disease during childhood.
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Cri-du-chat syndrome is diagnosed in infants and young children on the basis of clinical symptoms and may be confirmed through chromosomal analysis.
It may be detected prior to birth through prenatal of affected individuals.It is important to continue regular visits with the child's providers after leaving the hospital. Genetic counseling and testing is recommended for all people with a family history of this syndrome. Review Date: 8/4/2011Reviewed By: Chad Haldeman-Englert, MD, Wake Forest University School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Also reviewed by David Zieve, MD, MHA, Medical Director, A. is accredited by URAC, also known as the American Accreditation Health Care Commission (org). It was first described by French geneticist (ocular hypertelorism), and a failure to thrive.