Cri du chat syndrome
Definition
Cri du chat syndrome is a group of symptoms that result from missing a piece of chromosome number 5. The syndrome’s name is based on the infant’s cry, which is high-pitched and sounds like a cat.
Alternative Names
Chromosome 5p deletion syndrome; 5p minus syndrome; Cat cry syndrome
Causes
Cri du chat syndrome is rare. It is caused by a problem with chromosome 5.
Most cases are believed to occur during the development of the egg or sperm. A small number of cases occur when a parent passes a different, rearranged form of the chromosome onto their child.
Symptoms
Exams and Tests
The doctor will perform a physical exam. This may show:
Genetic tests can show a missing part of chromosome 5. Skull x-ray may reveal an problems with the shape of the base of the skull.
Treatment
There is no specific treatment. Your doctor will suggest ways to treat or manage the symptoms.
Parents of a child with this syndrome should have genetic counseling and testing to determine if one parent has a change in chromosome 5.
Support Groups
5p- Society -- www.fivepminus.org
Outlook (Prognosis)
Intellectual disability (mental retardation) is common. Half of children with this syndrome learn enough verbal skills to communicate. The cat-like cry becomes less noticeable over time.
Possible Complications
Complications depend on the amount of intellectual disability (mental retardation) and physical problems. Symptoms may affect the person's ability to care for themself.
When to Contact a Medical Professional
This syndrome is usually diagnosed at birth. Your health care provider will discuss your baby's symptoms with you. It is important to continue regular visits with the child's health care providers after leaving the hospital.
Genetic counseling and testing is recommended for all persons with a family history of this syndrome.
Prevention
There is no known prevention. Couples with a family history of this syndrome who wish to become pregnant may consider genetic counseling.
References
Descartes M, Carroll AJ. Cytogenetics. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 18th Ed. Philadelphia, Pa: Saunders Elsevier; 2007: chap 81.
Review Date:
8/4/2011
Reviewed By:
Chad Haldeman-Englert, MD, Wake Forest University School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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