Q fever

Q fever, caused by <i>Coxiella burnetii</i>, is a bacterial zoonosis with a wide clinical spectrum that can be life-threatening and, in some cases, can become chronic.



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Narrow down the case reports



Total: 357 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(57.1%)
9810369
[Coxiella burnetii endocarditis. A report of the first case diagnosed in Mexico].
Sahagun Sanchez G, Cotter Lemus L, Zamora Gonzalez C, Reyes PA, Ramirez S, Buendia A.
Arch Inst Cardiol Mex. 1998;68(4):322-7.
Splenomegaly Anemia Fever Hepatomegaly
Antibodies, Bacterial Bacterial Endocarditis Child Combined Modality Therapy Coxiella burnetii Echocardiography Females Homo sapiens Mexico Q Fever
1
(57.1%)
3958826
Chronic Q fever endocarditis with massive splenomegaly in childhood.
Laufer D, Lew PD, Oberhansli I, Cox JN, Longson M.
J Pediatr. 1986;108(4):535-9.
Hepatosplenomegaly Splenomegaly Anemia Fever
Antibodies, Bacterial Bacterial Endocarditis Child, Preschool Coxiella Cross Infection Echocardiography Females Hepatomegaly Homo sapiens Pulmonary Hypertension Q Fever Respirovirus Infections Splenomegaly Tetralogy of Fallot Ventricular Septal Defects
3
(50.9%)
11695318
[Prosthetic valve endocarditis due to Coxiella burnetii: six cases].
Auzary C, Pinganaud C, Launay O, Joly V, Cremieux AC, Idatte JM, Carbon C.
Rev Med Interne. 2001;22(10):948-58.
Congestive heart failure Splenomegaly Anemia Hepatomegaly
Adult Anti-Bacterial Agents Bacterial Endocarditis Coxiella burnetii Differential Diagnosis Echocardiography Females Heart Valve Prosthesis Homo sapiens Male Q Fever
4
(49.7%)
18971160
Acute Q fever presenting as fever of unknown origin with rapidly progressive hepatic failure in a patient with alcoholism.
Lin PH, Lo YC, Chiang FT, Wang JL, Jeng YM, Fang CT, Chang SC.
J Formos Med Assoc. 2008;107(11):896-901.
Jaundice Fever Hepatomegaly Prolonged prothrombin time
Alcoholic Intoxication, Chronic Fever of Unknown Origin Homo sapiens Liver Failure, Acute Male Middle Aged Q Fever
5
(49.1%)
19522308
[A case report of acute Q fever showing Kawasaki disease-like symptoms in a 9-year-old girl].
Ohgimi C, Tanaka R, Oh-ishi T.
Kansenshogaku Zasshi. 2009;83(3):245-50.
Anemia Fever Erythema
CRP TRIM21
Acute Disease Child Differential Diagnosis Females Homo sapiens Mucocutaneous Lymph Node Syndrome Q Fever
6
(48.7%)
8049325
[Hepatic granulomatosis caused by Q fever: a cause of erroneous tuberculosis diagnosis].
Arrebola Garcia JD, Magro Ledesma D, Montero Leal C, Vera Tome A, Perez Miranda M.
An Med Interna. 1993;10(12):595-8.
Anemia Fever Hepatic granulomatosis
Acute Disease Adult Anemia Bronchiolitis Diagnostic Errors Differential Diagnosis Fever of Unknown Origin Granuloma Homo sapiens Male Q Fever Respiratory Insufficiency Tuberculoma Tuberculosis, Hepatic
7
(46.2%)
19577708
Severe Q fever community-acquired pneumonia (CAP) mimicking Legionnaires' disease: Clinical significance of cold agglutinins, anti-smooth muscle antibodies and thrombocytosis.
Cunha BA, Nausheen S, Busch L.
Heart Lung. 2009;38(4):354-62.
Splenomegaly Thrombocytosis Hypophosphatemia Hepatomegaly
Adult Autoantibodies Biological Markers Community-Acquired Infections Cryoglobulins Differential Diagnosis Females Homo sapiens Legionnaires' Disease Pneumonia, Bacterial Q Fever Thrombocytosis
8
(45.3%)
23402798
Q fever and Mediterranean spotted fever associated with hemophagocytic syndrome: case study and literature review.
Lecronier M, Prendki V, Gerin M, Schneerson M, Renvoise A, Larroche C, Ziol M, Fain O, Mekinian A.
Int J Infect Dis. 2013;17(8):e629-33.
Splenomegaly Hypertriglyceridemia Hemophagocytosis
Adult Aged, 80 and over Biopsy Boutonneuse Fever Child Child, Preschool Females Homo sapiens Liver Lymphohistiocytosis, Hemophagocytic Lymphoma Male Middle Aged Q Fever Retrospective Studies Young Adult
9
(44.2%)
26167830
[Brucellosis as a cause of hemophagocytic syndrome].
Aydn S, Gunal O, Taskn MH, Atilla A, Klc SS.
Mikrobiyol Bul. 2015;49(2):292-4.
Hepatosplenomegaly Fever Hemophagocytosis
Agricultural Workers' Diseases Anti-Bacterial Agents Bacteremia Brucella melitensis Brucellosis Coombs Test Homo sapiens Lymphohistiocytosis, Hemophagocytic Male
9
(44.2%)
21453973
Recurrent fever of unknown origin (FUO): aseptic meningitis, hepatosplenomegaly, pericarditis and a double quotidian fever due to juvenile rheumatoid arthritis (JRA).
Cunha BA, Hage JE, Nouri Y.
Heart Lung. 2012;41(2):177-80.
Hepatosplenomegaly Leukemia Fever
Aseptic Meningitis Body Temperature Differential Diagnosis Fever of Unknown Origin Hepatomegaly Homo sapiens Magnetic Resonance Imaging Male Pericarditis Splenomegaly Young Adult
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 98

HPO ID Term # of case reports
HP:0100584 Endocarditis 118
HP:0012115 Hepatitis 42
HP:0001945 Fever 41
HP:0002090 Pneumonia 39
HP:0032252 Granuloma 17
HP:0002754 Osteomyelitis 15
HP:0004942 Aortic aneurysm 11
HP:0012819 Myocarditis 9
HP:0025615 Abscess 9
HP:0000099 Glomerulonephritis 7
HP:0001082 Cholecystitis 7
HP:0002315 Headache 6
HP:0001287 Meningitis 5
HP:0001701 Pericarditis 5
HP:0005112 Abdominal aortic aneurysm 5
HP:0012378 Fatigue 5
HP:0001744 Splenomegaly 4
HP:0100653 Optic neuritis 4
HP:0200119 Acute hepatitis 4
HP:0001369 Arthritis 3
HP:0001647 Bicuspid aortic valve 3
HP:0001894 Thrombocytosis 3
HP:0005268 Spontaneous abortion 3
HP:0005521 Disseminated intravascular coagulation 3
HP:0031035 Chronic infection 3
HP:0000112 Nephropathy 2
HP:0000952 Jaundice 2
HP:0000979 Purpura 2
HP:0001370 Rheumatoid arthritis 2
HP:0001399 Hepatic failure 2
HP:0001824 Weight loss 2
HP:0001876 Pancytopenia 2
HP:0001955 Unexplained fevers 2
HP:0002113 Pulmonary infiltrates 2
HP:0002721 Immunodeficiency 2
HP:0003326 Myalgia 2
HP:0012490 Panniculitis 2
HP:0025142 Constitutional symptom 2
HP:0100778 Cryoglobulinemia 2
HP:0200123 Chronic hepatitis 2
HP:0000083 Renal insufficiency 1
HP:0000618 Blindness 1
HP:0000822 Hypertension 1
HP:0001250 Seizures 1
HP:0001271 Polyneuropathy 1
HP:0001396 Cholestasis 1
HP:0001511 Intrauterine growth retardation 1
HP:0001562 Oligohydramnios 1
HP:0001622 Premature birth 1
HP:0001629 Ventricular septal defect 1
HP:0001634 Mitral valve prolapse 1
HP:0001653 Mitral regurgitation 1
HP:0001662 Bradycardia 1
HP:0001873 Thrombocytopenia 1
HP:0001908 Hypoplastic anemia 1
HP:0001909 Leukemia 1
HP:0001954 Recurrent fever 1
HP:0001970 Tubulointerstitial nephritis 1
HP:0002027 Abdominal pain 1
HP:0002196 Myelopathy 1
HP:0002240 Hepatomegaly 1
HP:0002326 Transient ischemic attack 1
HP:0002381 Aphasia 1
HP:0002586 Peritonitis 1
HP:0002616 Aortic root aneurysm 1
HP:0002716 Lymphadenopathy 1
HP:0002719 Recurrent infections 1
HP:0002758 Osteoarthritis 1
HP:0002829 Arthralgia 1
HP:0002835 Aspiration 1
HP:0002840 Lymphadenitis 1
HP:0002878 Respiratory failure 1
HP:0002904 Hyperbilirubinemia 1
HP:0002955 Granulomatosis 1
HP:0002960 Autoimmunity 1
HP:0003095 Septic arthritis 1
HP:0003201 Rhabdomyolysis 1
HP:0003470 Paralysis 1
HP:0004420 Arterial thrombosis 1
HP:0005305 Cerebral venous thrombosis 1
HP:0006562 Viral hepatitis 1
HP:0011419 Placental abruption 1
HP:0011955 Hepatic granulomatosis 1
HP:0012156 Hemophagocytosis 1
HP:0012219 Erythema nodosum 1
HP:0012223 Splenic rupture 1
HP:0012387 Bronchitis 1
HP:0012432 Chronic fatigue 1
HP:0012727 Thoracic aortic aneurysm 1
HP:0012735 Cough 1
HP:0025143 Chills 1
HP:0025145 Rigors 1
HP:0030955 Alcoholism 1
HP:0031002 Neuritis 1
HP:0031245 Productive cough 1
HP:0040313 Oligoarthritis 1
HP:0100646 Thyroiditis 1
HP:0100806 Sepsis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID