exudative polyserositis - meaning and definition. What is exudative polyserositis
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What (who) is exudative polyserositis - definition

HUMAN DISEASE
Familial Mediteranian Fever; Mediterranean fever, familial; Benign paroxysmal peritonitis; Wolff Periodic disease; Familial paroxysmal polyserositis; Polyserositis; Familial Mediterranean Fever; Erevan disease; Familial mediterranean fever; Periodic peritonitis; Recurrent polyserositis; Periodic disease; Reimann periodic disease; Siegal-Cattan-Mamou disease; Armenian disease
  • Erysipeloid rashes in Familial Mediterranean Fever

Familial exudative vitreoretinopathy         
  • Laser photocoagulation involves using a laser to cauterize the portions of retina which are not supplied by blood vessels.
RETINAL VASCULAR DISEASE CHARACTERIZED BY THE PREVENTION OF BLOOD VESSEL FORMATION AT THE EDGES OF THE RETINA AND THE HEMORRHAGE OF THE BLOOD VESSELS IN THE RETINA
Exudative vitreoretinopathy
Familial exudative vitreoretinopathy (FEVR, pronounced as fever) is a genetic disorder affecting the growth and development of blood vessels in the retina of the eye. This disease can lead to visual impairment and sometimes complete blindness in one or both eyes.
Familial Mediterranean fever         
Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder. FMF is an autoinflammatory disease caused by mutations in Mediterranean fever gene, which encodes a 781–amino acid protein called pyrin.
Coats' disease         
  • A young child with the yellow eye of Coats' disease - still in an early stage. Only visible with a flash camera.
Coats' disease is a rare congenital, nonhereditary eye disorder, causing full or partial blindness, characterized by abnormal development of blood vessels behind the retina. Coats' disease can also fall under glaucoma.

Wikipedia

Familial Mediterranean fever

Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder.: 149  FMF is an autoinflammatory disease caused by mutations in Mediterranean fever gene, which encodes a 781–amino acid protein called pyrin. While all ethnic groups are susceptible to FMF, it usually occurs in people of Mediterranean origin—including Sephardic Jews, Mizrahi Jews, Ashkenazi Jews, Assyrians, Armenians, Azerbaijanis, Levantines, Kurds, Greeks, Turks and Italians.

The disorder has been given various names, including familial paroxysmal polyserositis, periodic peritonitis, recurrent polyserositis, benign paroxysmal peritonitis, periodic disease or periodic fever, Reimann periodic disease or Reimann syndrome, Siegal-Cattan-Mamou disease, and Wolff periodic disease. Note that "periodic fever" can also refer to any of the periodic fever syndromes.