The Disease Of Behcet s Disease - 924 Words

In 1937, a rare disease called Behcet s Disease (BD) was first described by Dr. Hulusi Behcet, who is a dermatologist in Turkey. The disease is also known as Behcet s syndrome and described by The American Behcet s Disease Association (2014) as a rare, chronic, autoimmune, autoinflammatory disorder (American Behcet s Disease Association [ABDA], 2014). The disease, recognized worldwide, can affect multiple systems in the human body and associated with morbidity and mortality. Dr. Hulusi Behcet (2014) first described the disease as a triad of oral ulcers, genital ulcers and ocular inflammation (ABDA, 2014). The epidemiology behind this disease indicates its prevalence in multiple countries. It is less prevalent in the United States and Western Europe. According to National Organization for Rare Disorders (2015),the highest prevalence rate, 80-370 cases per 100,000, of this disease is in Turkey, as well as in Japan, Korea, China, Iran and Saudi Arabia (National Organization for Rare Dis orders [NORD], 2015). According to the National Institute of Arthritis and Musculoskeletal and Skin Disease, the disease affects more men than women in Middle Eastern and Asian countries. However, it affects more women than men in the United States (National Institute of Arthritis and Musculoskeletal and Skin Disease [NIAMS], 2015). It can develop in people of all ages but it tends to develop in people between the ages of 20 to 40. The Behcet s disease symptoms vary from personShow MoreRelatedGenetic Factors And Its Effects On The Silk Road763 Words   |  4 Pagesprevalence of BD varied between 20 and 421 per 100 000 in adults with a higher frequency detected in Anatolia compared to Europe [12]. BD is considered as both autoimmune disease and autoinflammatory disorder. It is thought that common environmental factors play a role in development of BD, however it is suggested that onset of disease occurs only in genetically predisposed individuals. Genetic factors have been scrutinized widely in BD. Familial aggregation studies in patients with BD suggest a strongRead MoreOrganizing Pneumonia Associated With Anticonvulsant Hypersensitivity Syndrome Induced By Lamotrigine1405 Words   |  6 Pagesthe left lung (Figure1). She was treated as infectious pneumonia with oral antibiotic. She started to have respiratory distress and needed oxygen to maintain her saturation. We obtained a chest CT which revealed multifocal patchy areas of airspace disease with ground glass-haziness appearance on both lower lobes with mediastinal lymphadenopathy and pleural effusion (Figures 2, 3 4). Her temperature continued to spike and she deteriorated in her respiratory status, worsening neutropenia, anemia andRead MoreCase Study of a Patient with Periodontal Disease Essay2081 Words   |  9 Pagesuse or smoking cessation, genetic predisposition, immunology, haematinic deficiency (iron, folate and vitamin B12), underlying systemic disorders, skin disorders or autoimmune diseases. (Scully, Medical Problems in Dentistry, 2010). Some may result due to malignant conditions and few may be due to underlying systemic diseases. In this case there is evidence to support this lesion is pertaining to that of a recurrent aphthous ulcer, as the patient is a non-smoker and reports to suffer anxiety. Additionally