"Cri-du-Chat Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-).
| Descriptor ID |
D003410
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| MeSH Number(s) |
C10.597.606.643.180 C16.131.077.262 C16.131.260.190 C16.320.180.190
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| Concept/Terms |
Cri-du-Chat Syndrome- Cri-du-Chat Syndrome
- Cri du Chat Syndrome
- Cri-du-Chat Syndromes
- Syndrome, Cri-du-Chat
- Syndromes, Cri-du-Chat
- Chromosome 5p- Syndrome
- 5p- Syndrome, Chromosome
- 5p- Syndromes, Chromosome
- Chromosome 5p- Syndromes
- Syndrome, Chromosome 5p-
- Syndromes, Chromosome 5p-
- 5p Deletion Syndrome
- 5p Deletion Syndromes
- Deletion Syndrome, 5p
- Deletion Syndromes, 5p
- Syndrome, 5p Deletion
- Syndromes, 5p Deletion
- 5p Minus Syndrome
- 5p Minus Syndromes
- Minus Syndrome, 5p
- Minus Syndromes, 5p
- Syndrome, 5p Minus
- Syndromes, 5p Minus
- Deletion of Short Arm of Chromosome 5 Syndrome
- 5p- Syndrome
- 5p Syndrome
- 5p- Syndromes
- Syndrome, 5p-
- Chromosome 5p Deletion Syndrome
- Cat Cry Syndrome
- Cat Cry Syndromes
- Syndrome, Cat Cry
- Syndromes, Cat Cry
- Crying Cat Syndrome
- Crying Cat Syndromes
- Syndrome, Crying Cat
- Syndromes, Crying Cat
- Chromosome 5 Short Arm Deletion Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Cri-du-Chat Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Cri-du-Chat Syndrome".
This graph shows the total number of publications written about "Cri-du-Chat Syndrome" by people in this website by year, and whether "Cri-du-Chat Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Cri-du-Chat Syndrome" by people in Profiles.
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Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory. Am J Obstet Gynecol. 2017 12; 217(6):691.e1-691.e6.
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Co-segregation of Freiberg's infraction with a familial translocation t(5;7)(p13.3;p22.2) ascertained by a child with cri du chat syndrome and brachydactyly type A1B. Am J Med Genet A. 2015 Feb; 167A(2):445-9.
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Anaesthetic considerations for the patient with cri du chat syndrome. Paediatr Anaesth. 1995; 5(2):139-41.