- Cri du chat
Cri du chat or Cri-du-chat Classification and external resources
Facial features of a patient with Cri du Chat syndrome at age of 8 months (A), 2 years (B), 4 years (C) and 9 years (D)
ICD-10 Q93.4 ICD-9 758.31 OMIM 123450 DiseasesDB 29133 MedlinePlus 001593 eMedicine ped/504
Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p minus syndrome or Lejeune’s syndrome, is a rare genetic disorder due to a missing part of chromosome 5. Its name is a French term (cat-cry or call of the cat) referring to the characteristic cat-like cry of affected children. It was first described by Jérôme Lejeune in 1963. The condition affects an estimated 1 in 50,000 live births, strikes all ethnicities, and is more common in females by a 4:3 ratio.
Signs and symptoms
The syndrome gets its name from the characteristic cry of affected infants, which is similar to that of a meowing kitten, due to problems with the larynx and nervous system. About 1/3 of children lose the cry by age 2. Other symptoms of cri du chat syndrome may include:
- feeding problems because of difficulty swallowing and sucking.
- low birth weight and poor growth.
- severe cognitive, speech, and motor delays.
- behavioral problems such as hyperactivity, aggression, tantrums, and repetitive movements.
- unusual facial features which may change over time.
- excessive drooling.
Other common findings include hypotonia, microcephaly, growth retardation, a round face with full cheeks, hypertelorism, epicanthal folds, down-slanting palpebral fissures, strabismus, flat nasal bridge, down-turned mouth, micrognathia, low-set ears, short fingers, single palmar creases, and cardiac defects (e.g., ventricular septal defect [VSD], atrial septal defect [ASD], patent ductus arteriosus [PDA], tetralogy of Fallot). People with Cri du chat are fertile and can reproduce.
Less frequently encountered findings include cleft lip and palate, preauricular tags and fistulas, thymic dysplasia, intestinal malrotation, megacolon, inguinal hernia, dislocated hips, cryptorchidism, hypospadias, rare renal malformations (e.g., horseshoe kidneys, renal ectopia or agenesis, hydronephrosis), clinodactyly of the fifth fingers, talipes equinovarus, pes planus, syndactyly of the second and third fingers and toes, oligosyndactyly, and hyperextensible joints. The syndrome may also include various dermatoglyphics, including transverse flexion creases, distal axial triradius, increased whorls and arches on digits, and a single palmar crease.
Late childhood and adolescence findings include significant intellectual disability, microcephaly, coarsening of facial features, prominent supraorbital ridges, deep-set eyes, hypoplastic nasal bridge, severe malocclusion, and scoliosis.
Affected females reach puberty, develop secondary sex characteristics, and menstruate at the usual time. The genital tract is usually normal in females except for a report of a bicornuate uterus. In males, testes are often small, but spermatogenesis is thought to be normal.
Cri du chat syndrome is due to a partial deletion of the short arm of chromosome number 5, also called "5p monosomy". Approximately 90% of cases results from a sporadic, or randomly-occurring, de novo deletion. The remaining 10-15% are due to unequal segregation of a parental balanced translocation where the 5p monosomy is often accompanied by a trisomic portion of the genome. These individuals may have more severe disease than those with isolated monosomy of 5p.
Most cases involve total loss of the most distant 20-10% of the material on the short arm. Fewer than 10% of cases have other rare cytogenetic aberrations (e.g., interstitial deletions, mosaicisms, rings and de novo translocations). The deleted chromosome 5 is paternal in origin in about 80% of de novo cases.
Loss of a small region in band 5p15.2 (cri du chat critical region) correlates with all the clinical features of the syndrome with the exception of the catlike cry, which maps to band 5p15.3 (catlike critical region). The results suggest that 2 noncontiguous critical regions contain genes involved in this condition's etiology. Two genes in these regions, Semaphorine F (SEMA5A) and delta catenin (CTNND2), are potentially involved in cerebral development. The deletion of the telomerase reverse transcriptase (hTERT) gene localized in 5p15.33 may contribute to the phenotypic changes in cri du chat syndrome as well.
Diagnosis and management
Diagnosis is based on the distinctive cry and accompanying physical problems. Genetic counseling and genetic testing may be offered to families with individuals who have cri du chat syndrome. Prenatally the deletion of the Cri du chat related region in the p arm of chromosome 5 can be detected from amniotic fluid or chronionic villi samples with BACs-on-Beads technology. Children may be treated by speech, sound, and occupational therapists. Cardiac abnormalities often require surgical correction.
- ^ Lejeune J, Lafourcade J, Berger R, et al. (1963). "[3 Cases of partial deletion of the short arm of chromosome 5]" (in French). C. R. Hebd. Seances Acad. Sci. 257: 3098–102. PMID 14095841.
- ^ ped/504 at eMedicine
- Spanish Support Group
- Australian Support Group
- United States Support Group
- United Kingdom Support Group
- A documentation in word and pictures: 24 years of living with the cri du chat-syndrome
Pathology: chromosome abnormalities (Q90–Q99 · 758) Autosomal1q21.1 deletion syndrome/1q21.1 duplication syndrome/TAR syndrome (1) · Wolf-Hirschhorn syndrome (4) · Cri du chat/Chromosome 5q deletion syndrome (5) · Williams syndrome (7) · Jacobsen syndrome (11) · Miller–Dieker syndrome/Smith–Magenis syndrome (17) · DiGeorge syndrome (22) · 22q13 deletion syndrome (22)
genomic imprinting (Angelman syndrome/Prader–Willi syndrome (15))Distal 18q-/Proximal 18q-
X/Y linked TranslocationsLymphoidMyeloidOther Other
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Look at other dictionaries:
Cri-du-chat — Klassifikation nach ICD 10 Q93.4 Deletion des kurzen Armes des Chromosoms 5 Katzenschrei Syndrom … Deutsch Wikipedia
cri du chat — /kree dooh shah , dyooh/. See cat s cry syndrome. [ < F: lit., cry of the cat] * * * cri du chat , cri du chat syndrome /krē dü shäˈ (sinˈdrōm)/ noun A rare, often fatal, congenital condition, so called because underdevelopment of the larynx… … Useful english dictionary
cri du chat — /kree dooh shah , dyooh/. See cat s cry syndrome. [ < F: lit., cry of the cat] * * * … Universalium
cri du chat — (kre doo shahґ) [Fr. â€œcat s cryâ€] see under syndrome … Medical dictionary
Cri-du-chat-Syndrom — Cri du chat Syn|drom* [kridy ʃa...] das; s <zu fr. cri du chat »Katzenschrei«, wegen des im Säuglingsalter auftretenden Schreiens, das durch diese Krankheit bedingt ist> Katzenschreisyndrom, eine Erbkrankheit mit Gesichts , Schädel u.… … Das große Fremdwörterbuch
Cri-du-Chat-Syndrom — [kridy ʃa , französisch], das Katzenschreisyndrom … Universal-Lexikon
cri du chat syndrome — krē du̇ shä , də n an inherited condition characterized by a mewing cry, mental retardation, physical anomalies, and the absence of part of a chromosome called also cat cry syndrome * * * a hereditary congenital syndrome characterized by hypertel … Medical dictionary
Cri-du-chat-Syndrom — Klassifikation nach ICD 10 Q93.4 Deletion des kurzen Armes des Chromosoms 5 Katzenschrei Syndrom … Deutsch Wikipedia
Cri-du-chat Syndrom — Klassifikation nach ICD 10 Q93.4 Deletion des kurzen Armes des Chromosoms 5 Katzenschrei Syndrom … Deutsch Wikipedia
cri du chat syndrome — ˌkrēdu̇ˈshä , dəˈ noun Etymology: cri du chat from French, cry of the cat : an inherited condition that is characterized by a mewing cry, mental retardation, physical anomalies, and the absence of part of a chromosome * * * cri du chat , cri du… … Useful english dictionary