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Cri du Chat syndrome: a case report.

Carolina Paes Torres1, Maria Cristina Borsatto, Alexandra Mussolino de Queiroz

  • 1Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Brazil. caroltorres@forp.usp.br

Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry
|February 9, 2006
PubMed
Summary

Cri du Chat Syndrome, a genetic disorder from chromosome 5 deletion, causes developmental issues. This case report details the dental care for a 23-year-old patient with this syndrome.

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Area of Science:

  • Genetics
  • Pediatrics
  • Dentistry

Background:

  • Cri du Chat Syndrome is a rare genetic disorder caused by a partial deletion on the short arm of chromosome 5.
  • It is characterized by a distinct catlike cry in infancy, intellectual disability, and distinctive facial features.

Observation:

  • The case report focuses on a 23-year-old patient diagnosed with Cri du Chat Syndrome.
  • The patient presented with various health issues including dental malocclusions, a common feature of the syndrome.

Findings:

  • The study highlights the importance of multidisciplinary treatment for individuals with Cri du Chat Syndrome.
  • Dental treatment, alongside special education and early stimulation, is crucial for managing the syndrome's complexities.

Implications:

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  • This case underscores the need for comprehensive, long-term care plans for Cri du Chat Syndrome patients.
  • Effective management can improve the quality of life and functional outcomes for individuals with this genetic condition.