MCID: SYR007
MIFTS: 15

Syringohydromyelia

Categories: Neuronal diseases

Aliases & Classifications for Syringohydromyelia

MalaCards integrated aliases for Syringohydromyelia:

Name: Syringohydromyelia 54

Classifications:



Summaries for Syringohydromyelia

NINDS : 54 Hydromyelia refers to an abnormal widening of the central canal of the spinal cord that creates a cavity in which cerebrospinal fluid (commonly known as spinal fluid) can accumulate.  As spinal fluid builds up, it may put abnormal pressure on the spinal cord and damage nerve cells and their connections.  Hydromyelia is sometimes used interchangeably with syringomyelia, the name for a condition that also involves cavitation in the spinal cord.  In hydromyelia, the cavity that forms is connected to the fourth ventricle in the brain, and is almost always associated in infants and children with hydrocephalus or birth defects such as Chiari Malformation II and Dandy-Walker syndrome.  Syringomyelia, however, features a closed cavity and occurs primarily in adults, the majority of whom have Chiari Malformation type 1 or have experienced spinal cord trauma.   Symptoms, which may occur over time, include weakness of the hands and arms, stiffness in the legs; and sensory loss in the neck and arms. Some individuals have severe pain in the neck and arms. Diagnosis is made by magnetic resonance imaging (MRI), which reveals abnormalities in the anatomy of the spinal cord..

MalaCards based summary : Syringohydromyelia is related to syringomyelia, noncommunicating isolated and syringomyelia. Affiliated tissues include spinal cord, brain and lung.

Related Diseases for Syringohydromyelia

Diseases related to Syringohydromyelia via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 68)
# Related Disease Score Top Affiliating Genes
1 syringomyelia, noncommunicating isolated 10.4
2 syringomyelia 10.4
3 scoliosis 10.4
4 hydrocephalus 10.4
5 congenital hydrocephalus 10.4
6 myelomeningocele 10.3
7 ataxia and polyneuropathy, adult-onset 10.3
8 chiari malformation 10.3
9 hydromyelia 10.3
10 arachnoid cysts 10.2
11 lipomatosis, multiple 10.2
12 spinal arachnoiditis 10.2
13 diastematomyelia 10.2
14 pleomorphic lipoma 10.2
15 arachnoiditis 10.2
16 split spinal cord malformation 10.2
17 chiari malformation type i 10.1
18 neural tube defects 10.1
19 meningocele 10.1
20 neurogenic arthropathy 10.1
21 arthropathy 10.1
22 benign ependymoma 10.1
23 ependymoma 10.1
24 syringobulbia 10.1
25 hajdu-cheney syndrome 9.9
26 anorectal anomalies 9.9
27 epidermoid cysts 9.9
28 ige responsiveness, atopic 9.9
29 myelopathy, htlv-1-associated 9.9
30 hemifacial microsomia 9.9
31 proteus syndrome 9.9
32 van buchem disease 9.9
33 meningioma, radiation-induced 9.9
34 meningioma, familial 9.9
35 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.9
36 cloacal exstrophy 9.9
37 sensorineural hearing loss 9.9
38 cysticercosis 9.9
39 spinal meningioma 9.9
40 osteopetrosis 9.9
41 obstructive hydrocephalus 9.9
42 central neurocytoma 9.9
43 papilledema 9.9
44 ventricular septal defect 9.9
45 heart septal defect 9.9
46 exostosis 9.9
47 lipomatosis 9.9
48 tropical spastic paraparesis 9.9
49 vestibular disease 9.9
50 cranial nerve palsy 9.9

Graphical network of the top 20 diseases related to Syringohydromyelia:



Diseases related to Syringohydromyelia

Symptoms & Phenotypes for Syringohydromyelia

Drugs & Therapeutics for Syringohydromyelia

Search Clinical Trials , NIH Clinical Center for Syringohydromyelia

Genetic Tests for Syringohydromyelia

Anatomical Context for Syringohydromyelia

MalaCards organs/tissues related to Syringohydromyelia:

41
Spinal Cord, Brain, Lung, Bone, Tonsil

Publications for Syringohydromyelia

Articles related to Syringohydromyelia:

(show top 50) (show all 174)
# Title Authors PMID Year
1
Schwannosis in Three Foals and a Calf. 38
31109258 2019
2
Management opinions from different centers (Rio de Janeiro). 38
31093731 2019
3
Distal Arthrogryposis with Impaired Proprioception and Touch: Description of an Early Phenotype in a Boy with Compound Heterozygosity of PIEZO2 Mutations and Review of the Literature. 38
30800044 2019
4
Unprecedented complication of odontoid regeneration after transoral odontoidectomy. 38
30783355 2018
5
Characterization of spinal cord diffusion tensor imaging metrics in clinically asymptomatic pediatric subjects with incidental congenital lesions. 38
29928513 2018
6
Syringohydromyelia in Patients with Chiari I Malformation: A Retrospective Analysis. 38
28684453 2017
7
Spinal capillary hemangiomas: Two cases reports and review of the literature. 38
28761543 2017
8
Multiple neural tube defects: a rare combination of limited dorsal myeloschisis, diplomyelia with dorsal bony spur, sacral meningocoele, syringohydromyelia, and tethered cord. 38
27942921 2017
9
Suspected drug-induced infiltrative lung disease culminating in acute respiratory failure in a dog treated with cytarabine and prednisone. 38
27062671 2016
10
Delayed Onset Intracranial Subdural Hematoma Following Spinal Surgery. 38
27192649 2016
11
Does medical therapy influence the size of the syrinx in dogs with Chiari-like malformation/syringohydromyelia complex? 38
27045274 2016
12
Chiari Malformations and Syringohydromyelia in Children. 38
27063663 2016
13
Parasitic twin--a supernumerary limb associated with spinal malformations. A case report. 38
26811301 2016
14
PROGRESSIVE SYRINGOHYDROMYELIA AND DEGENERATIVE AXONOPATHY IN A BOBCAT (LYNX RUFUS) FOLLOWING SURGICAL CORRECTION OF A CHIARI-LIKE MALFORMATION. 38
27010296 2016
15
Digenic mutations of human OCRL paralogs in Dent's disease type 2 associated with Chiari I malformation. 38
28018608 2016
16
Spontaneous regression of a chiari malformation type 1 in a 58-year-old female. 38
30459999 2016
17
Retrospective multicenter evaluation of the "fly-catching syndrome" in 24 dogs: EEG, BAER, MRI, CSF findings and response to antiepileptic and antidepressant treatment. 38
26584225 2015
18
Management of idiopathic pediatric syringohydromyelia. 38
26207665 2015
19
Acute onset of postoperative syringohydromyelia. 38
26557165 2015
20
Neuroimaging and the clinical manifestations of Chiari Malformation Type I (CMI). 38
26017710 2015
21
Syringohydromyelia in association with syringobulbia and syringocephaly: case report. 38
26030334 2015
22
MRI characteristics of fourth ventricle arachnoid diverticula in five dogs. 38
25385344 2015
23
Syringomyelia with Chiari I malformation presenting as hip charcot arthropathy: a case report and literature review. 38
25692057 2015
24
Magnetic resonance imaging features of complex Chiari malformation variant of Chiari 1 malformation. 38
24898393 2014
25
Compressive Cervicothoracic Adhesive Arachnoiditis following Aneurysmal Subarachnoid Hemorrhage: A Case Report and Literature Review. 38
25083391 2014
26
Cervical spinal intradural arachnoid cysts in related, young pugs. 38
24372140 2014
27
Imaging of Chiari type I malformation and syringohydromyelia. 38
24287386 2014
28
Imaging of the craniovertebral junction anomalies in children. 38
24265045 2014
29
Differentiation between intramedullary spinal ependymoma and astrocytoma: comparative MRI analysis. 38
24034546 2014
30
Blood stream infection by an emerging pathogen Oligella ureolytica in a cancer patient: case report and review of literature. 38
24739856 2014
31
Spinal neurocytoma with extensive syringohydromyelia. 38
24132448 2013
32
[Prenatal MRI as a method of controlling fetal pathology]. 38
24032261 2013
33
Arnold-Chiari 1 malformation type 1 with syringohydromyelia presenting as acute tetraparesis: a case report. 38
23809533 2013
34
Ultrasonographic diagnosis of syringohydromyelia and segmental hypoplasia of the lumbar spinal cord in a calf. 38
23039936 2012
35
Cervicothoracic syringohydromyelia associated with a prosencephalic mass in a dog. 38
23013378 2012
36
Comparison of the relative occipital bone volume between Cavalier King Charles spaniels with and without syringohydromyelia and French bulldogs. 38
22702890 2012
37
Rhombencephalosynapsis - isolated anomaly or complex malformation? 38
23049579 2012
38
Experimental syringohydromyelia induced by adhesive arachnoiditis in the rabbit: changes in the blood-spinal cord barrier, neuroinflammatory foci, and syrinx formation. 38
22439613 2012
39
Syringosubarachnoid shunt as a management for syringohydromyelia in dogs. 38
22417093 2012
40
Amelioration of caudal thoracic syringohydromyelia following surgical management of an adjacent arachnoid cyst. 38
22122126 2012
41
Mean displacement map of spine and spinal cord disorders using high b-value q-space imaging-feasibility study. 38
22067205 2011
42
Resolution of syringohydromyelia with targeted CT-guided epidural blood patching. 38
21529136 2011
43
Teaching NeuroImages: Acquired Chiari malformation with syringohydromyelia caused by posterior fossa. 38
21844530 2011
44
Dermoid sinus and spina bifida in three dogs and a cat. 38
21627660 2011
45
Syringohydromyelia in horses: 3 cases. 38
21532819 2011
46
Duraplasty or not? An evidence-based review of the pediatric Chiari I malformation. 38
20890606 2011
47
Magnetic resonance imaging in the evaluation of the fetal spinal canal contents. 38
20188501 2011
48
Cervical myelocystocele: Case report and review of literature. 38
21977091 2011
49
Teaching NeuroImages: acquired Chiari malformation with syringohydromyelia caused by posterior fossa tumor. 38
20921506 2010
50
Concurrent occipital hypoplasia, occipital dysplasia, syringohydromyelia, and hydrocephalus in a Yorkshire terrier. 38
21037897 2010

Variations for Syringohydromyelia

Expression for Syringohydromyelia

Search GEO for disease gene expression data for Syringohydromyelia.

Pathways for Syringohydromyelia

GO Terms for Syringohydromyelia

Sources for Syringohydromyelia

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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