MCID: RVR002
MIFTS: 22

Reversible Cerebral Vasoconstriction Syndrome malady

Categories: Rare diseases, Neuronal diseases

Aliases & Classifications for Reversible Cerebral Vasoconstriction Syndrome

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Aliases & Descriptions for Reversible Cerebral Vasoconstriction Syndrome:

Name: Reversible Cerebral Vasoconstriction Syndrome 45 51 65
 
Rcvs 45 51

Characteristics:

Orphanet epidemiological data:

51
reversible cerebral vasoconstriction syndrome:
Inheritance: Not applicable; Age of onset: Adult

Classifications:



External Ids:

Orphanet51 284388
UMLS65 C3544214

Summaries for Reversible Cerebral Vasoconstriction Syndrome

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Wikipedia:68 Reversible cerebral vasoconstriction syndrome (RCVS, sometimes called Call-Fleming syndrome) is a... more...

MalaCards based summary: Reversible Cerebral Vasoconstriction Syndrome, also known as rcvs, is related to thyroiditis and lung cancer. Affiliated tissues include brain, colon and retina.

Related Diseases for Reversible Cerebral Vasoconstriction Syndrome

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Graphical network of the top 20 diseases related to Reversible Cerebral Vasoconstriction Syndrome:



Diseases related to reversible cerebral vasoconstriction syndrome

Symptoms for Reversible Cerebral Vasoconstriction Syndrome

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Drugs & Therapeutics for Reversible Cerebral Vasoconstriction Syndrome

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Interventional clinical trials:

idNameStatusNCT IDPhase
1Perfusion MRI in Reversible Cerebral Vasoconstriction SyndromeNot yet recruitingNCT02756416

Search NIH Clinical Center for Reversible Cerebral Vasoconstriction Syndrome

Genetic Tests for Reversible Cerebral Vasoconstriction Syndrome

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Anatomical Context for Reversible Cerebral Vasoconstriction Syndrome

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MalaCards organs/tissues related to Reversible Cerebral Vasoconstriction Syndrome:

33
Brain, Colon, Retina, Endothelial, B cells, T cells, Myeloid

Animal Models for Reversible Cerebral Vasoconstriction Syndrome or affiliated genes

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Publications for Reversible Cerebral Vasoconstriction Syndrome

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Articles related to Reversible Cerebral Vasoconstriction Syndrome:

(show top 50)    (show all 144)
idTitleAuthorsYear
1
Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome. (26927259)
2016
2
Treatment Outcome and Prognostic Factors for Malignant Skin Melanoma Treated with Radical Surgery. (26320440)
2015
3
Piperlongumine induces apoptotic and autophagic death of the primary myeloid leukemia cells from patients via activation of ROS-p38/JNK pathways. (25619389)
2015
4
Heterelogous expression of mutated HLA-G decreases immunogenicity of human embryonic stem cells and their epidermal derivatives. (25218797)
2014
5
High expression of long non-coding RNA SPRY4-IT1 predicts poor prognosis of clear cell renal cell carcinoma. (25337221)
2014
6
The emerging role of SHANK genes in neuropsychiatric disorders. (24124131)
2014
7
Schizophrenia and retinitis pigmentosa: are there mechanisms which blind insanity? (22826378)
2013
8
Urinary heme oxygenase-1 in children with congenital hydronephrosis due to ureteropelvic junction obstruction. (22630328)
2012
9
Correction of dog dystrophic epidermolysis bullosa by transplantation of genetically modified epidermal autografts. (21697889)
2011
10
Posterior kyphectomy for myelomeningocele with anterior placement of fixation: a retrospective review. (20949380)
2011
11
Evaluation of spasticity in children with cerebral palsy using Ashworth and Tardieu Scales compared with laboratory measures. (20223745)
2010
12
The protein tyrosine phosphatase PTP1B is required for efficient delivery of N-cadherin to the cell surface. (20181825)
2010
13
Horner's syndrome, Pseudo-Horner's syndrome, and simple anisocoria. (17764630)
2007
14
Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study. (17472988)
2007
15
Progress in the study on mammalian diacylgycerol acyltransgerase (DGAT) gene and its biological function]. (17905705)
2007
16
An alternatively spliced transcript of the PHD3 gene retains prolyl hydroxylase activity. (16473674)
2006
17
Both the phosphoinositide and receptor binding activities of Dab1 are required for Reelin-stimulated Dab1 tyrosine phosphorylation. (16046028)
2005
18
Location and timing of initial osteoid deposition in postmeningitic labyrinthitis ossificans determined by multiple fluorescent labels. (15064623)
2004
19
Improvement of insulin resistance and early atherosclerosis in patients after gastric banding. (14981221)
2004
20
Coexistence of BCL1/CCND1 and CMYC aberrations in blastoid mantle cell lymphoma: a rare finding associated with very poor outcome. (15138714)
2004
21
Leptin levels in female patients with restrictive and purgative types of anorexia nervosa]. (12920794)
2003
22
Human CD30: structural implications from epitope mapping and modeling studies. (12557237)
2003
23
Enteroinsular axis of db/db mice and efficacy of dipeptidyl peptidase IV inhibition. (12524666)
2003
24
In acute inflammation, the chondroitin-4 sulphate carried by bikunin is not only longer, it is also undersulphated. (12765780)
2003
25
Activation of mitogen-activated protein kinases during granulocyte apoptosis in patients with severe sepsis. (12412617)
2002
26
The role of blood component removal in essential and reactive thrombocytosis. (11886575)
2002
27
Selective upregulation of endothelin B receptor gene expression in severe pulmonary hypertension. (11877350)
2002
28
Protein kinase C regulates transcription of the human guanylate cyclase C gene. (11277940)
2001
29
Internodal specializations of myelinated axons in the central nervous system. (11512672)
2001
30
Fibromyalgia, chronic fatigue syndrome, and myofascial pain syndrome. (11224736)
2001
31
Peripartum cardiomyopathy. (11372016)
2001
32
Characterization of the Ca2+-binding sites of annexin II tetramer. (10980196)
2000
33
Advances in nutritional management of chronic pancreatitis. (10981031)
2000
34
Lipoprotein disorder in brain infarction and hemorrhage. (9594362)
1998
35
Human estrogen sulfotransferase (hEST1) activities and its mRNA in various breast cancer cell lines. Effect of the progestin, promegestone (R-5020). (9749835)
1998
36
DD genotype of the angiotensin I-converting enzyme gene is a risk factor for early onset of essential hypertension in Japanese patients. (9626985)
1998
37
"Response to Hord and Janco re chemotherapy for unresectable pancreatoblastoma". (9212854)
1997
38
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene. (9222238)
1997
39
Stimulation of Ca2+ influx in alpha T3-1 gonadotrophs via the cAMP/PKA signaling system. (9374669)
1997
40
Swine influenza virus strains recognize sialylsugar chains containing the molecular species of sialic acid predominantly present in the swine tracheal epithelium. (9119062)
1997
41
Selective expression of T-cell receptor-V beta in acute infectious mononucleosis. (7605160)
1995
42
Determination of the glucurono-conjugated position in bile alcohol glucuronides excreted in urine of a patient with cerebrotendinous xanthomatosis by a nuclear magnetic resonance study. (8089079)
1994
43
Insulin-like growth factor I (IGF-I) and growth in children undergoing hemodialysis or after successful renal transplantation. (1820498)
1991
44
Cerebrospinal fluid proteins in men with chronic encephalopathy after exposure to organic solvents. (2284590)
1990
45
A study of 255 cases of granuloma inguinale. (3503822)
1987
46
Semilobar holoprosencephaly: embryologic, CSF dynamics and radiological considerations. (3962751)
1986
47
Pulmonary findings in patients with chagasic megaesophagus. Study of autopsied cases. (6401240)
1983
48
Central anticholinergic syndrome presenting as akinetic mutism. (22065382)
1981
49
Evaluation of erysipelas vaccines. (5030609)
1972
50
Cerebellar degeneration with clinical manifestation in chronic epileptic patients. (13903386)
1962

Variations for Reversible Cerebral Vasoconstriction Syndrome

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Expression for genes affiliated with Reversible Cerebral Vasoconstriction Syndrome

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Search GEO for disease gene expression data for Reversible Cerebral Vasoconstriction Syndrome.

Pathways for genes affiliated with Reversible Cerebral Vasoconstriction Syndrome

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GO Terms for genes affiliated with Reversible Cerebral Vasoconstriction Syndrome

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Sources for Reversible Cerebral Vasoconstriction Syndrome

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2CDC
14ExPASy
15FDA
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
34MedGen
36MeSH
37MESH via Orphanet
38MGI
41NCI
42NCIt
43NDF-RT
46NINDS
47Novoseek
49OMIM
50OMIM via Orphanet
54PubMed
55QIAGEN
60SNOMED-CT via Orphanet
64Tumor Gene Family of Databases
65UMLS
66UMLS via Orphanet