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Red ear syndrome (RES) is a rare disorder of unknown etiology which was originally described in 1994. The defining symptom of red ear syndrome is redness of one or both external ears, accompanied by a burning sensation. [1] A variety of treatments have been tried with limited success. [1]
Normal ear anatomy Earlobe creases seen in a Japanese angina patient. Frank's sign is a diagonal crease in the ear lobe extending from the tragus across the lobule to the rear edge of the auricle. [1] The sign is named after Sanders T. Frank. [1] It has been hypothesised that Frank's sign is indicative of cardiovascular disease [2] [3] and/or ...
A cauliflower ear deformity. Inflammation of the cartilage of the ear is a specific symptom of the disease and affects most people. [3] It is present in about 20% of persons with RP at presentation and in 90% at some point. [3] Both ears are often affected but the inflammation may alternate between either ear during a relapse. [3]
Some common symptoms and signs of mastoiditis include pain, tenderness, and swelling in the mastoid region. There may be ear pain , and the ear or mastoid region may be red (erythematous). Fever or headaches may also be present. Infants usually show nonspecific symptoms, including anorexia, diarrhea, or irritability. Drainage from the ear ...
Ear pain, also known as earache or otalgia, is pain in the ear. [1] [2] Primary ear pain is pain that originates from the ear. Secondary ear pain is a type of referred pain, meaning that the source of the pain differs from the location where the pain is felt. Most causes of ear pain are non-life-threatening.
Here are the symptoms to look for, plus how long you're contagious for, per an infectious disease doctor. Norovirus cases are surging in the US, the CDC says. Here are the symptoms to look for ...
The right ear is particularly special in spiritual traditions. As Stern tells us, "The right side of our body is our masculine side. Here is where logic, action and assertiveness live in the body."
Escher et al. described a family with dominantly inherited conductive deafness caused by ear anomalies in 1968 [5] and Wilmot et al. described another family with the same symptoms and mode of inheritance in 1970, [6] Schweitzer et al described the symptoms and declared a novel syndrome in 1984. [7]