Search your symptoms with MEDgle. You can check your symptoms. It is a medical symptom search allowing you find out what options make sense for you.
CLOSE
PATIENT GPS
patients
healthcare providers
how it works
about
login
edit search
new search
symptoms
diagnoses
physicians
drugs
procedures
close
symptoms
diagnoses
drugs
procedures
physicians
symptom duration
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
add symptom to current symptom search
same as above
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
add symptom to current symptom search
same as above
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
add symptom to current symptom search
same as above
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
gender
male
female
age
1-3
4-11
12-17
18-29
30-50
50+
age
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
calculate
visual
[hide visual search]
search visually
symptoms
|
diagnoses
|
drugs
|
procedures
|
physicians
search symptoms
•
Find causes for your symptoms
•
Discover relevant types of physicians
search diagnoses
•
Understand the details of a diagnosis
•
Learn about relevant tests and treatments
•
Find useful resources on the web
search drugs
•
Learn about different therapeutic drugs
•
Understand what they are used for
•
Know the potential options
search procedures
•
Learn about different diagnostic and therapeutic procedures
•
Understand what they are used for
•
Know the potential options
search physicians
•
Find physicians in your area
•
Understand what they do
•
Get the right help you need
reduced results from
132 B
21 M
2 M
741
704
to ~24 options
options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications
category
genetic or congenital
frequency
rare (U.S.)
likelihood by age
likelyhood by duration of symptoms
related physician types
family practitioner
internist
postal code
Find Local
The results are computer generated suggestions to help you find a physician. MEDgle does not recommend any particular type of physician or claim to be complete or accurate in the providers and specialties suggested.
cri-du-chat syndrome - syndrome that occurs from missing a piece of chromosome 5
Definition for Cri-du-chat Syndrome
Cri du chat syndrome (French for Cry or call of the cat), also called deletion 5p syndrome,5p minus or Le Jeune’s syndrome, is a rare genetic disorder due to a missing portion of chromosome 5.
more
Cri du chat syndrome (French for Cry or call of the cat), also called deletion 5p syndrome,5p minus or Le Jeune’s syndrome, is a rare genetic disorder due to a missing portion of chromosome 5. It was first described by Jérôme Lejeune in 1963. The condition affects an estimated 1 in 20,000 to 50,000 live births. The disorder is found in people of all ethnic backgrounds and is slightly more common in females.
less
some common symptoms
abnormal gait
behavioral changes
delayed development
difficulty speaking
some related diagnoses
1 - 7 of
24
diagnoses
neurofibromatosis type 1
urea cycle disorders
human immunodeficiency virus infections
intracranial arteriovenous malformations
hydrocephalus
myopathies
multiple sclerosis
more
do i have 'Cri-du-chat Syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'cri-du-chat syndrome'
1 - 5 of
14
diagnostic tests
ECHOcardiogram
Cri-du-chat Syndrome and ECHOcardiogram
X-ray skull
Cri-du-chat Syndrome and X-ray skull
X-rays
Cri-du-chat Syndrome and X-rays
Chromosomal analysis
Cri-du-chat Syndrome and Chromosomal analysis
Fluorescent in situ hybridization (FISH)
Cri-du-chat Syndrome and Fluorescent in situ hybridization (FISH)
Microarray-based comparative genomic hybridisation (array CGH)
Cri-du-chat Syndrome and Microarray-based comparative genomic hybridisation (array CGH)
Brain MRI
Cri-du-chat Syndrome and Brain MRI
Esophageal Manometry
Esophageal Motility
Cri-du-chat Syndrome and Esophageal Manometry
Gastroscopy
Cri-du-chat Syndrome and Gastroscopy
Swallowing studies
Cri-du-chat Syndrome and Swallowing studies
Developmental testing
Cri-du-chat Syndrome and Developmental testing
Videofluoroscopy swallowing
Cri-du-chat Syndrome and Videofluoroscopy swallowing
chromosomal microarray analysis
Cri-du-chat Syndrome and chromosomal microarray analysis
cine-esophagram
Cri-du-chat Syndrome and cine-esophagram
for more please login, login is free (click to login)
therapeutic procedures for 'Cri-du-chat Syndrome'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Cri-du-chat Syndrome:
therapeutic procedure search results for 'cri-du-chat syndrome'
1 - 1 of
1
therapeutic procedures
rankings are computer generated. please consult your health care provider.
Gastroscopy
Cri-du-chat Syndrome and Gastroscopy
medications search results for 'cri-du-chat syndrome'
rankings are computer generated. please consult your health care provider.
web search results for cri-du-chat syndrome
Web (All)
|
Treatment
|
Drugs
|
Tests
|
Research
|
Diet
Results
1 - 50
- Cri-du-chat Syndrome
[Cri-du-chat syndrome. A case report]
... case in Senegal with cri-du-chat syndrome diagnosed in a 3 ... Diagnosis of cri-du-chat syndrome is easy when characteristic cat-like-cry is present. ...
http://www.ncbi.nlm.nih.gov/pubmed/14666800
www.ncbi.nlm.nih.gov
-
summary
Cri-du-chat syndrome - MedlinePlus - Health information - Genetics Home ...
Genetic Conditions > cri-du-chat syndrome > MedlinePlus - Health information ... condition summary on cri-du-chat syndrome. Encyclopedia: Cri-du-Chat Syndrome ...
http://ghr.nlm.nih.gov/condition=criduchatsyndrome/show/MedlinePlus
ghr.nlm.nih.gov
-
summary
Cri-du-chat syndrome - Related Chromosome(s) - Genetics Home Reference
Genetic Conditions > cri-du-chat syndrome > Related Chromosome(s) chromosome 5 ... Lister Hill National Center for Biomedical Communications ...
http://ghr.nlm.nih.gov/condition=criduchatsyndrome/show/Related+Chromosome(s)
ghr.nlm.nih.gov
-
summary
Cri-du-chat syndrome: clinical profile and prenatal diagnosis.
Prenatal diagnosis of cri-du-chat syndrome is described in 2 pregnancies. ... Cri-du-Chat Syndrome/diagnosis* Cri-du-Chat Syndrome/genetics. Fatal Outcome. Female ...
http://www.ncbi.nlm.nih.gov/pubmed/10703584
www.ncbi.nlm.nih.gov
-
summary
Cri-du-chat syndrome - Related Gene(s) - Genetics Home Reference
Genetic Conditions > cri-du-chat syndrome > Related Gene(s) ... Lister Hill National Center for Biomedical Communications ... Department of Health & Human ...
http://ghr.nlm.nih.gov/condition=criduchatsyndrome/show/Related+Gene(s)
ghr.nlm.nih.gov
-
summary
Cri-du-chat syndrome - Educational resources - Information pages ...
... in the Genetics Home Reference condition summary on cri-du-chat syndrome. Ask the Geneticist: General information about cri-du-chat syndrome ...
http://ghr.nlm.nih.gov/condition=criduchatsyndrome/show/Educational+resources
ghr.nlm.nih.gov
-
summary
Cri-du-chat syndrome - Patient support - For patients and families ...
Genetic Conditions > cri-du-chat syndrome > Patient support - For patients and families ... in the Genetics Home Reference condition summary on cri-du-chat syndrome. ...
http://ghr.nlm.nih.gov/condition=criduchatsyndrome/show/Patient+support
ghr.nlm.nih.gov
-
summary
Antenatal sonographic features of cri-du-chat syndrome.
Antenatal sonographic features of cri-du-chat syndrome. Aoki S, Hata T, Hata K, Miyazaki K. ... Cri-du-Chat Syndrome/ultrasonography* Female. Fetal Death ...
http://www.ncbi.nlm.nih.gov/pubmed/10204218
www.ncbi.nlm.nih.gov
-
summary
Cri-du-chat syndrome - References - Genetics Home Reference
Cerruti Mainardi P. Cri du Chat syndrome. Orphanet J Rare Dis. ... Cornish K, Bramble D. Cri du chat syndrome: genotype-phenotype correlations and ...
http://ghr.nlm.nih.gov/condition=criduchatsyndrome/show/References
ghr.nlm.nih.gov
-
summary
Autosomal Deletion Syndromes
758.31 Cri-du-Chat (currently listed under 758.3) 758.32 Velo-Cardio-Facial Syndrome ... Cri-du-Chat syndrome. First recognized syndrome due to a deletion (1963) ...
http://www.cdc.gov/nchs/ppt/icd9/att4_1203.ppt
www.cdc.gov
-
summary
Heart and circulation - Genetics Home Reference
... 5p- Syndrome see cri-du-chat syndrome. Complete trisomy 13 syndrome see ... cri-du-chat syndrome. CTX see ... see cri-du-chat syndrome. Mowat-Wilson ...
http://www.ghr.nlm.nih.gov/ghr/conditionsByCategory/show/heartandcirculation
www.ghr.nlm.nih.gov
-
summary
2009 MeSH Tree Structures. C16 - Congenital, Hereditary, and Neonatal ...
Cri-du-Chat Syndrome [C16.131.077.262] De Lange Syndrome [C16.131.077.272] ... Cri-du-Chat Syndrome [C16.320.180.190] De Lange Syndrome [C16.320.180.210] ...
http://www.nlm.nih.gov/mesh/2009/mesh_trees/C16.html
www.nlm.nih.gov
-
summary
Cri du chat syndrome
Cri du chat syndrome is a group of symptoms that result from missing a piece of ... Cri du chat syndrome is rare. It occurs when a piece of information on ...
http://adam.about.com/encyclopedia/infectiousdiseases/Cri-du-chat-syndrome.htm
adam.about.com
-
summary
Cri du Chat Syndrome - Yahoo! Health
Important It is possible that the main title of the report Cri du Chat Syndrome is not the name you expected. Please check the synonyms listing to find the ...
http://health.yahoo.com/other-other/cri-du-chat-syndrome/healthwise--nord19.html
health.yahoo.com
-
summary
Crying, Age 3 and Younger -- Topic Overview
Crying is your child's first way of communicating. ... conditions, such as cri du chat ("cat's cry") syndrome or phenylketonuria (PKU) ...
http://www.webmd.com/parenting/tc/crying-age-3-and-younger-topic-overview?page=2
www.webmd.com
-
summary
Chromosomal Deletion Syndromes: Chromosomal Anomalies: Merck Manual ...
5p-Deletion (cri du chat syndrome) ... 4p-Deletion (Wolf-Hirschhorn syndrome) ... Prader-Willi syndrome (see Endocrine and Metabolic Disorders in Children: Secondary) ...
http://www.merck.com/mmpe/print/sec19/ch294/ch294f.html
www.merck.com
-
summary
MedlinePlus Medical Encyclopedia: Cri du chat syndrome
Cri du chat syndrome is a group of symptoms that result from missing a piece of ... Cri du chat syndrome is rare. It occurs when a piece of information on ...
http://www.nlm.nih.gov/medlineplus/ency/article/001593.htm
www.nlm.nih.gov
-
summary
The cat cry syndrome (5p-) in adolescents and adults.
Cri-du-Chat Syndrome*/blood. Cri-du-Chat Syndrome*/complications ... Cri-du-Chat Syndrome*/physiopathology. Dermatoglyphics. Female. Gait. Humans. Karyotyping ...
http://www.ncbi.nlm.nih.gov/pubmed/5173012
www.ncbi.nlm.nih.gov
-
summary
Cri-du-chat syndrome - Genetics Home Reference
Some children with cri-du-chat syndrome are also born with a heart defect. ... MedlinePlus Encyclopedia: Cri-du-Chat Syndrome ...
http://ghr.nlm.nih.gov/condition=criduchatsyndrome
ghr.nlm.nih.gov
-
summary
PATENT DUCTUS ARTERIOSUS - Pedbase.org
Trisomy-18, -13, -9, Cri-du-chat Syndrome; Charge and VATER Associations, ... Congenital Rubella Syndrome; Carpenter, Conradi, Crouzon, Smith-Limli-Opitz, ...
http://pedbase.org/p/patent-ductus-arteriosus_pda/
pedbase.org
-
summary
Two cases of deletion 5p syndrome: one with paternal involvement and ...
... of deletion 5p or cri du chat syndrome (CdCS) with different presentations and ... Cri-du-Chat Syndrome/diagnosis. Cri-du-Chat Syndrome/genetics* Gene Deletion ...
http://www.ncbi.nlm.nih.gov/pubmed/18418516?ordinalpos=40&it...
www.ncbi.nlm.nih.gov
-
summary
Mental Retardation (MR): Learning and Developmental Disorders: Merck ...
Cri du chat syndrome. Down syndrome. Fragile X syndrome. Klinefelter's syndrome ... syndrome (trisomy 21) via standard karyotyping, 5p-deletion (cri du chat ...
http://www.merck.com/mmpe/sec19/ch299/ch299e.html
www.merck.com
-
summary
MedlinePlus Medical Encyclopedia: Hearing loss
Leopard syndrome (multiple lentigines) Otosclerosis. Robinson type ectodermal dysplasia ... Rubella syndrome. Congenital atresia of the external auditory canal ...
http://www.nlm.nih.gov/medlineplus/ency/article/003044.htm
www.nlm.nih.gov
-
summary
[Wolf-Hirschhorn syndrome, cat cry syndrome]
Miura K, Niikawa N. Department of Human Genetics, Nagasaki University School of Medicine. ... Cri-du-Chat Syndrome* Female. Humans. Infant. Infant, Newborn. Male ...
http://www.ncbi.nlm.nih.gov/pubmed/9047986
www.ncbi.nlm.nih.gov
-
summary
Brain and nervous system - Genetics Home Reference
Chromosome 5p- Syndrome see cri-du-chat syndrome ... monosomy 5p see cri-du-chat syndrome. 17p11.2 monosomy see Smith-Magenis syndrome ...
http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/brainandnervoussystem
ghr.nlm.nih.gov
-
summary
Simian crease
Cri du chat syndrome. What to Expect at Your Office Visit ... and signs that, when taken together, define a specific syndrome or condition. ...
http://adam.about.com/encyclopedia/Simian-crease.htm
adam.about.com
-
summary
PMID 12162388
... 44 7 2002 Jul Cri du chat syndrome: genotype-phenotype correlations and ... genetics Chromosome Deletion Cri-du-Chat Syndrome diagnosis genetics therapy ...
http://www.ncbi.nlm.nih.gov/pubmed/12162388
www.ncbi.nlm.nih.gov
-
summary
MedlinePlus Medical Encyclopedia: Mental retardation
Chromosome deletions (cri du chat syndrome) ... Environmental. Deprivation syndrome. Genetic abnormalities and inherited metabolic disorders ...
http://www.nlm.nih.gov/MEDLINEPLUS/ency/article/001523.htm
www.nlm.nih.gov
-
summary
Neurologic Diseases - Genetics Home Reference
congenital central hypoventilation syndrome. Cornelia de Lange syndrome. cri-du-chat syndrome ... Menkes syndrome. metachromatic leukodystrophy ...
http://ghr.nlm.nih.gov/medlineplusTopic=neurologicdiseases
ghr.nlm.nih.gov
-
summary
Genotype-phenotype correlation of 5p-syndrome: pitfall of diagnosis.
Furthermore, one 5p- syndrome patient was diagnosed only by the ... Cri-du-Chat Syndrome/diagnosis* Cri-du-Chat Syndrome/genetics* Female. Genotype. Humans ...
http://www.ncbi.nlm.nih.gov/pubmed/15602631
www.ncbi.nlm.nih.gov
-
summary
Mental retardation
Chromosome deletions (cri du chat syndrome) ... Environmental. Deprivation syndrome. Genetic abnormalities and inherited metabolic disorders ...
http://adam.about.com/encyclopedia/infectiousdiseases/Mental-retardation.htm
adam.about.com
-
summary
Otitis Media (Chronic): Middle Ear and Tympanic Membrane Disorders ...
Chronic otitis media is a persistent, chronically draining (> 6 wk), suppurative ... with craniofacial abnormalities (eg, Down syndrome, cri du chat syndrome, cleft ...
http://www.merck.com/mmpe/print/sec08/ch087/ch087f.html
www.merck.com
-
summary
Encyclopedia C-Cz on Yahoo! Health
Health encyclopedia of diseases and conditions covering symptoms, definitions, alternative names, causes, ... Cri du Chat (5P) Syndrome. Cri du Chat ...
http://health.yahoo.com/ency/c/
health.yahoo.com
-
summary
Genetic Disease Glossary of Terms with Definitions on MedicineNet.com
Genetic Disease glossary includes a list of Genetic Disease related ... (p) arm from chromosome 5. Also called the cri du chat (or cri-du-chat) syndrome. ...
http://www.medicinenet.com/genetic_disease/glossary.htm
www.medicinenet.com
-
summary
123450
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123450
www.ncbi.nlm.nih.gov
-
summary
Chromosome 5 - Conditions related to genes on chromosome 5 - Genetics ...
Cornelia de Lange syndrome. craniometaphyseal dysplasia. cri-du-chat syndrome. Crohn disease. diastrophic dysplasia. Ehlers-Danlos syndrome ...
http://ghr.nlm.nih.gov/chromosome=5/show/Conditions
ghr.nlm.nih.gov
-
summary
MedlinePlus Medical Encyclopedia: Simian crease
Cri du chat syndrome. What to Expect at Your Office Visit Return to top ... and signs that, when taken together, define a specific syndrome or condition. ...
http://www.nlm.nih.gov/medlineplus/ency/article/003290.htm
www.nlm.nih.gov
-
summary
Cri du chat syndrome.
Cri du chat syndrome. Iyer SL, Duraiswamy A, Kher AS, Joshi S, Bharucha BA, Kanade S. ... Three cases of cri du chat syndrome with varying ages of presentation are ...
http://www.ncbi.nlm.nih.gov/pubmed/9715326
www.ncbi.nlm.nih.gov
-
summary
MedlinePlus Medical Encyclopedia: Topics beginning with 0-9
47 X-X-Y syndrome see Klinefelter syndrome. 5'-NT see 5'-nucleotidase. 5'-nucleotidase ... 5p minus syndrome see Cri du chat syndrome. Return to top ...
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_0-9.htm
www.nlm.nih.gov
-
summary
Site Map od Pedbase.org - The Pediatric Database
Pedbase Site Map. Pediatric. Site Map. Resources. Contact. PEDBASE.org - The Pediatric Database. A. B. C. D. E. F. G. H. I. J. K. L. M. N. O. P. R. S. T. U. V. W. X ...
http://pedbase.org/sitemap.html
pedbase.org
-
summary
Intellectual Disability / Mental Retardation 3, DD, NCBDDD, CDC
Information on mental retardation. Provided by the U.S. Centers for Disease ... genetic conditions (such as Cri-du-chat syndrome or Prader-Willi syndrome) ...
http://www.cdc.gov/ncbddd/dd/mr3.htm
www.cdc.gov
-
summary
CTNND2 - catenin (cadherin-associated protein), delta 2 (neural ...
cri-du-chat syndrome - associated with the CTNND2 gene ... People with cri-du-chat syndrome who do not have a deletion of the CTNND2 gene ...
http://ghr.nlm.nih.gov/gene=ctnnd2
ghr.nlm.nih.gov
-
summary
Prenatal diagnosis of cri du chat (5p-) syndrome i...[Prenat Diagn ...
Prenatal diagnosis of cri du chat (5p-) syndrome in association with isolated ... 64-6 A case of prenatally detected cri du chat syndrome (5p-) is reported. ...
http://www.ncbi.nlm.nih.gov/pubmed/11810654
www.ncbi.nlm.nih.gov
-
summary
MedlinePlus Medical Encyclopedia: Topics beginning with Cp-Cz
Cri du chat syndrome. Crib death see Sudden infant death syndrome. Crigler-Najjar syndrome ... CRPS see Complex regional pain syndrome. CRT see Heart pacemaker ...
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_Cp-Cz.htm
www.nlm.nih.gov
-
summary
[Crying cat syndrome discovered during a routine examination]
Chromosomes, Human, 4-5. Craniofacial Dysostosis. Cri-du-Chat Syndrome/diagnosis* Dermatoglyphics. Eyelids/abnormalities. Humans. Infant ...
http://www.ncbi.nlm.nih.gov/pubmed/4675135
www.ncbi.nlm.nih.gov
-
summary
Cri du chat - Wikipedia, the free encyclopedia
... features of a patient with Cri du Chat syndrome at age of 8 months ... A documentation in word and pictures: 21 years of living with the cri du chat-syndrome ...
http://en.wikipedia.org/wiki/Cri_du_chat
en.wikipedia.org
-
summary
Norton - ADAM
Search engine description ... Chediak-Higashi syndrome. Childhood cerebral ... Cri du chat syndrome. Cyanotic heart disease. DDH. De Toni-Fanconi syndrome ...
http://nortonhealthcare.adam.com/content.aspx?productId=112&...
nortonhealthcare.adam.com
-
summary
CRI DU CHAT SYNDROME - Pedbase.org
... Database - CRI DU CHAT SYNDROME. Pediatric Organization - Pedbase [at] Gmail.com. 1994 -2007 Pedbase.org. Powered by Database of Pediatrics- CRI DU CHAT SYNDROME ...
http://www.pedbase.org/c/cri-du-chat-syndrome
www.pedbase.org
-
summary
PMID 5895684
5895684 1966 11 27 1966 11 27 2004 11 17 0018-7348 1 5 1965 Deletion of short ... Aberrations Chromosome Disorders Cri-du-Chat Syndrome Dermatoglyphics Humans Jaw ...
http://www.ncbi.nlm.nih.gov/pubmed/5895684
www.ncbi.nlm.nih.gov
-
summary
Cri du Chat Syndrome
The Cri du Chat Syndrome, first described in 1963 by Lejeune et al., is a ... 5 Niebuhr E. The cri du chat syndrome. Epidemiology, cytogenetics and clinical features. ...
http://www.orpha.net/data/patho/GB/uk-criduchat.pdf
www.orpha.net
-
summary
show more
1
2
faq/about
|
disclaimer
|
privacy policy
|
terms of service
|
browse
|
beta
|
contact
|
API - Catalyst
MEDgle does not provide medical advice, diagnosis or treatment. Copyright 2006-2012, MEDgle Inc. All Rights Reserved. MEDgle is NOT affiliated with Google. Last Updated: Mar 14, 2012
This site complies to the
HONcode standard for trustworthy health
information:
verify here
.
Invited Sponsor for Communications Conference
Finalist -- search & reference
MEDgle has been selected for the 2009 Best of Business Award in the Medical research