Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
...
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Preferred term
Cri-du-Chat Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- 5p Deletion Syndrome
- 5p Deletion Syndromes
- 5p Minus Syndrome
- 5p Minus Syndromes
- 5p Syndrome
- 5p- Syndrome
- 5p- Syndrome, Chromosome
- 5p- Syndromes
- 5p- Syndromes, Chromosome
- Cat Cry Syndrome
- Cat Cry Syndromes
- Chromosome 5p Deletion Syndrome
- Chromosome 5p- Syndrome
- Chromosome 5p- Syndromes
- Chromosome 5 Short Arm Deletion Syndrome
- Crying Cat Syndrome
- Crying Cat Syndromes
- Deletion of Short Arm of Chromosome 5 Syndrome
- Deletion Syndrome, 5p
- Deletion Syndromes, 5p
- Minus Syndrome, 5p
- Minus Syndromes, 5p
- Syndrome, 5p-
- Syndrome, 5p Deletion
- Syndrome, 5p Minus
- Syndrome, Cat Cry
- Syndrome, Chromosome 5p-
- Syndrome, Crying Cat
- Syndromes, 5p Deletion
- Syndromes, 5p Minus
- Syndromes, Cat Cry
- Syndromes, Chromosome 5p-
- Syndromes, Crying Cat
Scope note
- 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-).
History note
- 1977; use CRYING CAT SYNDROME 1964-1976
In other languages
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Finnish
-
cri-du-chat
-
cri-du-chat -oireyhtymä
-
cri-du-chat -syndrooma
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kissanhuuto-syndrooma
-
kromosomin 5 lyhyen haaran deleetio
-
syndroma cri-du-chat
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Swedish
-
Cri-du-chatsyndrom
URI
http://www.yso.fi/onto/mesh/D003410
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