Fevers do not cause headaches directly. Generally speaking (with the exception of true migraines), both fevers and headaches are symptoms of underlying problems.
Tomato Fever According to a newspaper,the patients with tomato fever get red rashes on the skin almost the size of tomatoes. The fever is locally called "tomato fever" and some patients have mentioned worms coming out of the boils that develop on the rashes. There is no fever named as Tomato fever. Some place the sores on the face due to chiken gunia fever is called as Tomato fever.
mediterranean
Familial CJD, representing 5-15% of cases, is inherited in an autosomal dominant manner, meaning that either parent may pass along the disease to a child,
It means there is no fever. Febrile means having fever
An Armenian disease is an alternative name for familial Mediterranean fever, a hereditary inflammatory disorder.
Simple Answer ... genetics. Diseased that would fall into this category include Familial Mediterranean Fever, Tay-Sachs or Sickle Cell Anemia.
OF course there are white families w/ FMF. The Mediterranean is Italy, France, Greece as well as Arab and Jewish families. This is not a black disease out of Africa but blacks can also have FMF as well as any family who has a mixed ancestry which MOST folks in today's world do have. :-) fmf_support@yahoogroups.com Nancy
The Brucella bacteria are connected to Brucellosis. Brucellosis is also called Bang's disease, Crimean fever, Gibraltar fever, Malta fever, Maltese fever, Mediterranean fever, undulant fever and rock fever.
doctor Ihssan Rjoub. Princess Haya Biotechnology Center (PHBC) Jordan University of Science and Technology (JUST) P. O. Box (3030) Irbid 22110, Jordan Tel.: 00-962-2-7200600 Ext. 40571 Fax: 00-962-2-7200632 e-mail : phbc@just.edu.jo
Familial - album - was created in 2001.
Yellow fever & malaria.
DefinitionFamilial Mediterranean fever is a disorder passed down through families (inherited), which involves repeated fevers and inflammation that often affects the abdomen or lungs.Alternative NamesFamilial paroxysmal polyserositis; Periodic peritonitis; Recurrent polyserositis; Benign paroxysmal peritonitis; Periodic disease; Periodic feverCauses, incidence, and risk factorsFamilial Mediterranean fever is caused by a mutation in the MEFV gene. The condition usually affects people of Mediterranean ancestry, especially non-Ashkenazi (Sephardic) Jews, Armenians, and Arabs, although people from other ethnic groups may also be affected.This disease is very rare. Risk factors include a family history of familial Mediterranean fever or having Mediterranean ancestry.SymptomsSymptoms usually begin ages 5 and 15. Inflammation in the lining of the abdominal cavity, chest cavity, skin, or joints occurs, along with high fevers that usually peak in 12 to 24 hours. Attacks may vary in severity of symptoms. Patients are usually symptom-free between attacks.Symptoms may include:Abdominal painthat occurs repeatedly (recurrent)Chest pain that occurs repeatedlyFever or alternating chills and fever (relapsing)Recurrent joint painSkin lesions that are red and swollen and range from 5 - 20 cm in diameterSigns and testsThere is no specific test to diagnose this disease. Sometimes analysis of the chromosomes can help. Ruling out other possible diseases using laboratory tests or x-rays will help determine the diagnosis.Certain blood tests may be higher than normal when done during an attack. Tests may include:CeruloplasminC-reactive proteinErythrocyte sedimentation rate (ESR)FibrinogenlevelGenetic testingSerum haptoglobinWhite blood cell countTreatmentThe treatment for familial Mediterranean fever is treatment of symptoms. Colchicine, a medicine that reduces inflammation, may help during an attack and may prevent further attacks.Expectations (prognosis)There is no known cure for familial Mediterranean fever. Most people continue to have attacks, but the number and severity of attacks is different from person to person.ComplicationsDiscomfort is the primary complication. There is a risk of addiction to the narcotic pain relievers used to relieve symptoms.Amyloidosis(deposits of protein in different organs) is more common in patients with familial Mediterranean fever. Gallbladder disease may also occur.Calling your health care providerCall your health care provider if symptoms develop to rule out other possible causes and get appropriate treatment. See a pain specialist if there is chronic pain.ReferencesKastner DL. The systemic autoinflammatory diseases. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 282.
it could be FMF which is a fever that runs in family especially Mediterranean area characterized by fever not more than 38C for up to 2-4 days recurrent with abdominal pain mimic appendicitis or cholecyctitis
for problems of chronic insomnia and fever
Familial in medical terms means hereditary.
We invited my grandparents over for a familial Christmas dinner.