Viral myositis




Input patient's signs and symptoms


Narrow down the case reports



Total: 15 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(17.5%)
29962438
[Cytomegalovirus myositis complicated with hemophagocytic lymphohistiocytosis, acute renal failure, and colitis].
Matsuo K, Nishihara H, Koga M, Omoto M, Ogasawara J, Kawai M, Kanda T.
Rinsho Shinkeigaku. 2018;58(7):423-429.
Muscle weakness
Colitis Cytomegalovirus Cytomegalovirus Infections Homo sapiens Intestinal Perforation Lymphohistiocytosis, Hemophagocytic Middle Aged Myositis Virus Activation
1
(17.5%)
28819047
Unusual case of bilateral hand weakness.
Datta S, Cosgrove J, Alam T, Ford HL.
Pract Neurol. 2017;17(6):479-481.
Lethargy Myositis
Adult Hand Homo sapiens Influenza Influenza A Virus, H1N1 Subtype Male Muscle Weakness Myositis
1
(17.5%)
27164356
Recurrent rhabdomyolysis in a child. Case presentation.
Ertugrul S, Yolbas , Aktar F, Ylmaz K, Tekin R.
Arch Argent Pediatr. 2016;114(3):e192-4.
Rhabdomyolysis
Child, Preschool Homo sapiens Male Respiratory Syncytial Virus Infections Rhabdomyolysis
1
(17.5%)
26952148
(4762789)
Isolated left upper extremity myositis and severe rhabdomyolysis in an adult with H1N1 Influenza, a case report with literature review.
Agrawal A, Razjouyan H, Atluri P, Patel A, Eng M.
IDCases. 2014;1(3):43-4.
Fever Rhabdomyolysis
1
(17.5%)
23546352
(3579047)
Three cases of acute myositis in adults following influenza-like illness during the H1N1 pandemic.
Gibson SB, Majersik JJ, Smith AG, Bromberg MB.
J Neurosci Rural Pract. 2013;4(1):51-4.
Elevated serum creatine kinase Myositis
1
(17.5%)
23304613
(3523589)
A case report on parvovirus b19 associated myositis.
Oliver ND, Millar A, Pendleton A.
Case Rep Rheumatol. 2012;2012:250537.
Myopathy
1
(17.5%)
21905081
A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emia.
Okamoto Y, Higuchi I, Sakiyama Y, Tokunaga S, Watanabe O, Arimura K, Nakagawa M, Takashima H.
Ann Neurol. 2011;70(3):486-92.
Muscle weakness
Adult Creatine Kinase DNA, Mitochondrial Databases, Genetic Disease Progression Females Genetic Polymorphism Hepatitis B, Chronic Homo sapiens Immunohistochemistry Japan Male Middle Aged Mitochondrial Diseases Muscle Weakness Myopathy Pain
1
(17.5%)
21730808
Recurrent viral-induced compartment syndrome.
Slobogean BL, Reilly CW, Alvarez CM.
Pediatr Emerg Care. 2011;27(7):660-2.
Rhabdomyolysis
Child Females Homo sapiens Influenza Influenza A Virus, H1N1 Subtype Myositis Rhabdomyolysis
1
(17.5%)
16538844
[A patient with serious viral myositis following flu].
Hoeksma M, van Baasbank MC, Remijn JA, Ruijs GJ, Veenhuizen L.
Ned Tijdschr Geneeskd. 2006;150(8):436-9.
Nephritis Rhabdomyolysis
Antibodies, Viral Differential Diagnosis Females Homo sapiens Influenza Myositis Nephritis Rhabdomyolysis
1
(17.5%)
11144172
[A patient of infantile polymyositis triggered by respiratory syncytium virus infection].
Nagasawa T, Sakuma H, Araki S, Watanabe A, Makino M, Nonaka I.
No To Hattatsu. 2000;32(6):543-6.
Pneumonia Generalized muscle weakness
Acute Disease Homo sapiens Infant Male Pneumonia, Viral Polymyositis Pulse Therapy, Drug Respiratory Insufficiency Respiratory Syncytial Virus Infections
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 9

HPO ID Term # of case reports
HP:0003201 Rhabdomyolysis 2
HP:0001260 Dysarthria 1
HP:0001324 Muscle weakness 1
HP:0001945 Fever 1
HP:0002015 Dysphagia 1
HP:0003198 Myopathy 1
HP:0003326 Myalgia 1
HP:0011947 Respiratory tract infection 1
HP:0100614 Myositis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID