National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Dengue Fever is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Breakbone Fever
- Dandy Fever
- Dengue Hemorrhagic Fever
- Dengue Shock Syndrome
- Seven Day Fever, Dengue Type
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
- Colorado Tick Fever
- Typhus (Typhoid Fever)
- Yellow Fever
- Other Hemorrhagic Fevers
Dengue Fever is an acute viral infection characterized by fever. It is caused by a bite from mosquitoes carrying dengue virus. The primary form of Dengue Fever is characterized by a skin rash and a high fever with severe pain in the head and muscles. Other symptoms may include shaking chills, diarrhea, and vomiting. Bouts of extreme exhaustion may last for months after the initial symptoms.
The secondary forms of this disorder are called Dengue Hemorrhagic Fever and Dengue Shock Syndrome. These usually are caused by a secondary infection with a different type of Dengue virus (Type 2), but may also be caused by the same virus that causes Dengue Fever. Several days after onset other symptoms may include fever, bleeding under the skin, red spots on the legs, and bleeding into the intestines. A marked fall in blood pressure (shock) occurs in very severe cases.
Dengue Fever is a disorder transmitted by female mosquitoes (Aedes aegypti and Aedes albopictus) carrying dengue virus. The disorder is characterized by a sudden onset of symptoms. There is an incubation period of 5 to 8 days after the mosquito bite occurs. The patient has chills or chilly sensations, a fever, exhaustion, diarrhea, and/or vomiting. Pain behind the eyeballs (postorbital) occurs on moving the head. The head, lower back, legs and joints ache. The patient feels very weak. The temperature rises rapidly, sometimes to as high as 40C or 104F, accompanied by a relatively slow heart beat (bradycardia) and abnormally low blood pressure. The lymph glands in the neck, shoulder, and groin are usually enlarged.
Two or three days after the first fever, a rash of flat or elevated (maculopapular) spots appears, particularly on the face. A second temperature rise follows. The presence of Dengue virus in the blood (viremia) can confirm the diagnosis. The patient subsequently develops immunity against this type of Dengue virus. However, reinfection with a different type of this virus is possible.
Secondary forms of Dengue Fever are Dengue Hemorrhagic Fever, and Dengue Shock Syndrome. These forms of the disorder primarily affect children between 3 and 6 years of age who have been infected a second time with dengue virus, and infants 7 to 8 months of age. These forms of the disorder are characterized by sudden fever, headache, nausea, vomiting, and abdominal pain. Coughing, throat infection and difficulty in breathing also occur. Shock may occur 2 to 6 days after the beginning of the fever, with sudden collapse, cool clammy extremities (the trunk is often warm), a weak pulse, and bluish discoloration of the skin around the mouth (cyanosis). In serious cases, a tendency to bleed excessively occurs, either as purpura or in pinpoint spots (petecchiae). The bleeding may appear in many parts of the body. Blood vessels become dilated and congested, and swelling (edema) may also occur. Gastrointestinal bleeding may lead to vomiting of blood (hematemesis) and passing of dark stools stained with blood pigment (melena).
Dengue Fever is caused by a virus that belongs to a family of viruses known as Flaviviruses. There is no vaccine, so travelers going to parts of the world where it is endemic during Dengue season (July to November) are urged to protect themselves from mosquito bites by wearing protective clothing and mosquito repellant.
Dengue Fever occurs mainly in subtropical or tropical climates including southern Asia, South America (particularly Brazil), and the Caribbean including Puerto Rico and the U.S. Virgin Islands. The virus has also been imported into the United States by tourists from these areas. It is thought that approximately 200 cases of Dengue Fever are unknowingly carried into the United States each year.
The Dengue virus is a B Arbovirus which has 4 distinct serogroups.
Colorado Tick Fever (Mountain Fever; Mountain Tick Fever) is a virus infection transmitted by ticks which is prevalent in the western United States. Fever, headaches, muscle aches, and generalized discomfort characterize the illness, which resolves spontaneously. (For more information on this disorder, choose "Colorado Tick Fever" as your search term in the Rare Disease Database.)
Epidemic Typhus (European Typhus; Classic Typhus; Louse-Born Typhus; Jail Fever) is a severe infectious disorder which begins suddenly and is characterized by prolonged high fever, persistent headache, and a rash of elevated spots on the skin. Epidemic Typhus is caused by Rickettsia prowazekii, an organism that resembles viruses and bacteria. This disorder can be transmitted by lice.
Yellow Fever is an arbovirus infection characterized by sudden onset and variable severity of symptoms. The disorder is characterized by a fever of 102 degrees to 104 F (39 degrees to 40 C), and an abnormally slow heart beat. In a few severe cases, excessive amounts of protein are present in the urine. In these few cases a yellow skin color (jaundice), bleeding and coughing up blood also tend to occur. The virus which causes Yellow Fever is transmitted by the bite of a mosquito. (For more information on this disorder, choose "Yellow Fever" as your search term in the Rare Disease Database.)
Other Hemorrhagic Fevers which are characterized by internal bleeding are caused by a variety of viruses. Some of these fevers that occur in Africa and South America are: Lassa Fever, Machupo Fever (Bolivian Hemorrhagic Fever), Junin Fever (Argentinian Hemorrhagic Fever), Lymphocytic Choriomeningitis, Marburg Virus (Hemorrhagic Fever), and, Ebola Virus (Hemorrhagic Fever). Blood tests may be used to identify the virus.
Dengue fever is diagnosed by testing a blood sample for the presence of the dengue virus or its antibodies, specifically immunoglobulin M (IgM).
The FDA approved in 2011 the first test (DENV Detect IgM Capture ELISA) to help diagnose people with signs and symptoms of dengue fever or dengue hemorrhagic fever. This test, patented by the US Centers for Disease Control and Prevention (CDC) and manufactured by InBios International, detects antibodies to dengue virus in blood samples from patients. IgM antibody response to the dengue virus infection is not detectable until 3-5 days after the onset of fever, which can produce a negative test result even though a person has dengue. During this "IgM negative window" the dengue virus is present in the bloodstream.
In 2012, the FDA approved a new diagnostic test (DENV-1-4 Real Time RT PCR Assay) developed by the CDC to detect the presence of dengue virus in people. This is the first approved assay that detects the dengue virus itself and can be performed using equipment and supplies that many public health laboratories already use to diagnose influenza. This test will permit earlier diagnosis of dengue virus infection, thus reducing the risk of death with timely care.
Complete bedrest is important. Affected individuals should take measures to avoid additional mosquito bites in order to prevent reinfection. Fluids should be given to compensate for dehydration.
Treatment for Dengue Hemorrhagic Fever depends on the individual's degree of dehydration. Affected individuals should be closely monitored to prevent shock. When skin appears bluish in color, oxygen should be given. Collapse of blood vessels and loss of fluid from the circulation (hemoconcentration) require immediate fluid replacement, preferably with a solution like Ringer's lactate. Plasma or human serum protein (albumin) should also be given if there is no response in the first hour. Fresh blood or blood platelet transfusions may control bleeding. Agitated patients may be given paraldehyde, chloral hydrate, or diazepam.
Scientists have studied the effect of human interferon on Hemorrhagic Dengue Fever. More research is needed before this drug will be available for more general use in treating Dengue Fever. Additionally, scientists are trying to develop a vaccine that may someday prevent this infectious disorder.
A pharmaceutical company known as Genelabs Technologies, Inc., is working on an RNA-binding drug program that has produced several compounds that potentially inhibit viral activity. It is hoped that this might lead to drug treatment options for RNA viruses, including yellow fever, hepatitis C, Japanese encephalitis, and Dengue fever. More research is necessary to develop and test such drugs for safety and long-term effectiveness.
Researchers at OraVax, Inc., plan to create vaccines against several forms of Dengue Fever by modifying a proven Yellow Fever vaccine. Genes from one of several types of Dengue Fever viruses will replace a gene in a Yellow Fever virus. Vaccines from the modified Yellow Fever virus will be tested for safety and efficacy against the Dengue Fever virus.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Branch SL, et al., Evaluation of four methods for detection of immunoglobulin M antibodies to dengue virus. Clin Diagn Lab Immunol. 1999;6:555-7.
Wali JP, et al., Dengue haemorrhagic fever in adults: a prospective study of 110 cases. Trop Doct. 1999;29:27-30.
Badiaga S, et al., Imported dengue: study of 44 cases observed from 1994 to 1997 in 9 university hospital centers. Infectio-Sud-France group. Pathol Biol. 1999;47:539-42.
Soler M, Laboratory diagnosis to dengue virus infections. Acta Cient Venez. 1998;49:25-32.
Alvarez ME, et al., Dengue and hepatic failure. American Journal Med. 1985;79:670-4.
Bancroft WH, et al., Dengue virus type 2 vaccine: reactogenicity and immunogenicity in soldiers. Journal Infect Dis. 1984;149:1005-10.
Hotta H, et al., Effect of interferons on Dengue virus multiplication in cultured monocytes/macrophages. Biken Journal. 1984;27:189-93.
Malison M, et al., Dengue fever in the United States. A report of a cluster of imported cases and review of the clinical, epidemiologic, and public health aspects of the disease. JAMA. 1983;249:496-500.
Centers for Disease Control and Prevention
1600 Clifton Road NE
Atlanta, GA 30333
NIH/National Institute of Allergy and Infectious Diseases
NIAID Office of Communications and Government Relations
5601 Fishers Lane, MSC 9806
Bethesda, MD 20892-9806
World Health Organization (WHO)
Avenue Appia 20
Geneva 27, 1211
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into myCigna.com. For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email firstname.lastname@example.org
Last Updated: 7/9/2012
Copyright 1988, 1989, 1995, 1999, 2000, 2001, 2009 National Organization for Rare Disorders, Inc.
Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.