Cri-du-chat Syndrome: Multimedia

References

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Further Reading

Guidelines are available for the clinical genetic evaluation of the child with mental retardation or developmental delays.

Keywords

cat cry syndrome, chromosome deletion 5p syndrome, monosomy 5p syndrome, (Bp-), 5p-, partial deletion of chromosome 5p, 5p deletion, 5p monosomy, growth failure, microcephaly, facial abnormalities, mental retardation, catlike cry, mewing cry, laryngeal hypoplasia, floppy epiglottis, small larynx, asymmetric vocal cords, pneumonia, congenital heart defects, respiratory distress syndrome, cri-du-chat syndrome, aneuploidies, feeding problems, failure to thrive, ear infections, cognitive delay, speech delay, motor delay, hyperactivity, self-injurious behavior, hypotonia, hypertelorism, epicanthal folds, down-slanting palpebral fissures, strabismus, down-turned mouth, flat nasal bridge, micrognathia, low-set ears, short fingers, single palmar creases, cardiac defects

cleft lip and palate, preauricular tags, preauricular fistulas, thymic dysplasia, gut malrotation, megacolon, inguinal hernia, dislocated hips, cryptorchidism, hypospadias, renal malformations, clinodactyly of the fifth fingers, talipes equinovarus, pes planus, syndactyly of the second and third fingers and toes, oligosyndactyly, hyperextensible joints, short philtrum, malocclusion of the teeth, scoliosis, short third-fifth metacarpals, transverse flexion creases, distal axial triradius

Contributor Information and Disclosures

Author

Harold Chen, MD, MS, FAAP, FACMG, Professor, Departments of Pediatrics, Obstetrics and Gynecology, and Pathology, Director of Genetic Laboratory Services, Louisiana State University Medical Center
Harold Chen, MD, MS, FAAP, FACMG is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society of Human Genetics, and Teratology Society
Disclosure: Nothing to disclose.

Medical Editor

Ian Krantz, MD, Department of Pediatrics, Assistant Professor, University of Pennsylvania and Children's Hospital of Philadelphia
Ian Krantz, MD is a member of the following medical societies: American Society of Human Genetics
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

David Flannery, MD, FAAP, FACMG, Vice Chair of Education, Chief, Section of Medical Genetics, Professor, Department of Pediatrics, Medical College of Georgia
David Flannery, MD, FAAP, FACMG is a member of the following medical societies: American Academy of Pediatrics and American College of Medical Genetics
Disclosure: Nothing to disclose.

CME Editor

Paul D Petry, DO, FACOP, FAAP, Consulting Staff, Freeman Pediatric Care, Freeman Health System
Paul D Petry, DO, FACOP, FAAP is a member of the following medical societies: American Academy of Osteopathy, American Academy of Pediatrics, American College of Osteopathic Pediatricians, and American Osteopathic Association
Disclosure: Nothing to disclose.

Chief Editor

Bruce Buehler, MD, Professor, Department of Pediatrics, Pathology and Microbiology, Executive Director, Hattie B Munroe Center for Human Genetics and Rehabilitation, University of Nebraska Medical Center
Bruce Buehler, MD is a member of the following medical societies: American Academy for Cerebral Palsy and Developmental Medicine, American Academy of Pediatrics, American Association on Mental Retardation, American College of Medical Genetics, American College of Physician Executives, American Medical Association, and Nebraska Medical Association
Disclosure: Nothing to disclose.