Morbus stills syndrom

Adult-onset Still's disease (AOSD) is a form of Still's disease, a rare systemic autoinflammatory disease characterized by the classic triad of persistent high spiking fevers, joint pain, and a distinctive salmon-colored bumpy rash. The disease is considered a diagnosis of exclusion Age is the main risk factor for adult Still's disease, with incidence peaking twice: once from 15 to 25 years and again from 36 to 46 years. Males and females are equally at risk. Complications. Most complications from adult Still's disease arise from chronic inflammation of organs and joints. Joint destruction

Adult-onset Still's disease - Wikipedi

Das Still-Syndrom des Erwachsenen ist eine seltene, hoch fieberhafte rheumatische Systemerkrankung unbekannter Ätiologie und Pathogenese. In erster Linie sind junge Erwachsene zwischen dem 16. und.. Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disease characterized by high spiking fever, arthritis, salmon-pink maculopapular rash and multiple organ involvement. We report a case of an adult-onset Still's disease that meets Yamaguchi's criteria and presented with typical clinical manifestations Das Still-Syndrom stellt die systemische Verlaufsform der juvenilen idiopathischen Arthritis dar. 2 Epidemiologie. Die Inzidenz der juvenilen idiopathischen Arthritis (JIA) liegt bei 4-5 auf 100.000 Kinder. Jedes Jahr erkranken 750 bis 1000 Kinder an der JIA. Jedes zehnte Kind entwickelt ein Still-Syndrom Still's disease symptoms and signs include inflammation with high fever spikes, fatigue, salmon-colored rash, and/or arthritis. Read about Still's disease treatment, prognosis, diagnosis, and risk factors. Still's disease is also called systemic-onset juvenile idiopathic arthritis

Adult Still's disease - Symptoms and causes - Mayo Clini

All patients with adult-onset Still disease eventually develop persistent chronic arthritis even if fever and systemic symptoms have stopped. Stiffness, swelling and pain usually affects many joints but in particular the wrists may become severely deformed. How is the diagnosis of adult-onset Still disease made Stills syndrom: forekommer hyppigst hos børn og viser sig ved led- og muskelsmerter, ondt i halsen, udslæt, feber, hævede lymfeknuder samt et fald i antallet af hvide blodlegemer (se evt. leukopeni). Behandlingen foregår vha. NSAIDs, binyrebarkhormon samt evt. biologiske midler Syndrome study guide by mitja_klutzny includes 38 questions covering vocabulary, terms and more. Quizlet flashcards, activities and games help you improve your grades

Osler-Weber-Rendu syndrome (OWR) is a genetic blood vessel disorder that often leads to excessive bleeding. The syndrome affects about one in 5,000 people Morbihan syndrome was possibly first described in 1956 by Schimpf, who published four case reports on this subject from 1956 to 1960.[2-4] Unfortunately, none of these articles had any clinical photographs. Furthermore, the histopathological picture of these patients was characterized by granulomas, that are rarely present in Morbihan syndrome Request PDF on ResearchGate | Adulter Morbus Still - Neues zur Diagnostik und Therapie | Der adulte Morbus Still (Englisch: adult-onset Still's disease - AOSD) ist eine seltene auto. Ledderhose disease (plantar fibromatosis, Morbus Ledderhose) Ledderhose disease, also called Ledderhose's Disease (LD), plantar fibromas, or Morbus Ledderhose is a fibromatosis, like Dupuytren's contracture. When suffering from Ledderhose disease benign nodules grow at the arch of the foot

Crohn's disease is a type of inflammatory bowel disease (IBD) that may affect any part of the gastrointestinal tract from mouth to anus. Signs and symptoms often include abdominal pain, diarrhea (which may be bloody if inflammation is severe), fever, and weight loss WebMD looks at the causes, symptoms, and treatment of Cushing's syndrome, a condition in which your body produces too much of the hormone cortisol Das Still-Syndrom des Erwachsenen ist eine seltene autoinflammatorische Erkrankung. AOSD steht für den englischen Begriff Adult-onset Still's disease. Weitere Bezeichnungen für die Erkrankung sind Adulter Morbus Still und Morbus Still des Erwachsenen. Der Beginn der Erkrankung liegt oft zwischen dem 15. und 40. Lebensjahr [1, 2]

Der Adulte Morbus Still (AOSD = Aduld Onset Still Disease) ist eine schwere Autoimmunerkrankung und gehört zur Gruppe der entzündlich-rheumatischen Erkrankungen. Es ist eine sehr seltene Unterform der Rheumatoiden Arthritis und wurde nach dem Entdeckerarzt Georg Frederec Still (1868-1941) benannt. Morbus heißt übersetzt Krankheit The epidemiology, clinical features, and diagnosis of Sweet syndrome will be discussed here. Information on the treatment and prognosis of Sweet syndrome and an overview of other neutrophilic dermatoses are available separately. (See Sweet syndrome (acute febrile neutrophilic dermatosis): Management and prognosis and Neutrophilic dermatoses. Test zur Prüfung der Durchlässigkeit der tiefen Beinvenen und damit zur Differenzierung zwischen primärer und sekundärer Varikosis. Achtung: Perthes gibt es als Morbus, Syndrom, und Test! Dabei hat das eine mit dem anderen nicht unbedingt was zu tun Adult-onset Still's disease (AOSD) is an inflammatory systemic disease of unknown aetiology, this may occur in any age in the adult and is associated with a diverse array of clinical symptoms. Typical symptoms of the disease are fever, arthralgias or arthritis, myalgias, the typical skin rash, sore throat, hepatosplenomegaly, lymphadenopathy.

Der adulte Morbus Still (Adult onset Still's disease, AOSD

Cytokine Storm - A Complication of Adult-onset Still's Disease Abstract. The macrophage activation syndrome (MAS) is a potentially life-threatening complication and it is typically associated with rheumatologic or autoimmune diseases The colloquially still common term Morbus Sudeck was replaced by the term Complex Regional Pain Syndrome (CRPS). What is Sudeck's disease or the complex regional pain syndrome? Sudeck's disease causes inflammatory overheating, swelling and neuropathic pain on the arm or leg

The following article discusses two forms of rheumatic diseases: rheumatoid arthritis (RA) and Still's disease. Click now to study more about RA and Still's disease including their symptoms , clinical signs , diagnosis , complications as well as treatment and therapy Das Morbus Still Syndrom wird in Wikipedia oder auf anderen Portalen auch als Morbus Still des Erwachsenen bezeichnet, weil äußerst selten ein Kind betroffen ist. AOSD wie es ebenfalls genannt wird ist eine Erkrankung bei Erwachsenen, die eine Erkrankung des Immunsystems darstellt

A variant of the disease is seen in connection with the skin disease psoriasis, or in association with chronic inflammation of the intestine, such as Crohn's disease or ulcerative colitis. Bechterews disease is 3 times more common in men than in women, and typically affects younger adults aged 20-40 years Der adulte Morbus Still. Article. Still's disease was diagnosed in a 40-year-old patient as a cause of psycho-organic syndrome with complete disorientation and stupor, sensory and motor. With Behçet's disease as an intercurrent disease in pregnancy, the pregnancy does not have an adverse effect on the course of Behçet's disease and may possibly ameliorate its course. Still, there is a substantial variability in clinical course between patients and even for different pregnancies in the same patient

Request PDF on ResearchGate | Biologic treatments for adult-onset Still's disease | Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder that is a diagnosis of exclusion. It is. Adult-onset Still's disease: current challenges and future prospects Mariam Siddiqui,1 Michael S Putman,2 Anisha B Dua,1 1Department of Rheumatology, 2Department of Internal Medicine, The University of Chicago Medical Center, Chicago, IL, USA Abstract: Adult-onset Still's disease (AOSD) - a multi-systemic inflammatory condition characterized by high fevers, polyarthritis, an evanescent rash. Adult-onset Still's disease (AOSD) is an inflammatory disease characterized by high fevers, rash, sore throat, and joint pain.Several joints are often affected at the same time, and the joints are often stiff for several hours in the morning It is also called Wells syndrome. What does eosinophilic cellulitis look like? Typically eosinophilic cellulitis is preceded by itching or burning skin. It presents with markedly swollen nodules and plaques (lumps) with prominent borders Sweet's syndrome. Sweet's syndrome is an uncommon skin condition marked by a distinctive eruption of tiny bumps that enlarge and are often tender to the touch, usually appearing on your back, neck, arms or face

Tietze syndrome is an inflammation of the costochondral cartilages of the upper front of the chest that involves swelling of the joint. While both costochondritis and Tietze syndrome feature symptoms such as localized chest pain and tenderness, Tietze syndrome also causes swelling over the ribs and cartilage near the breastbone (sternum). Signs. Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis, is the most common chronic arthritic disease of childhood and corresponds to a group of different subtypes. Epidemiology The estimated incidence is ~13 per 100,00.. Sjögrens syndrom - årsager, symptomer og behandling . Sjögrens syndrom (el. Sjøgrens) er en gigtsygdom og en bindevævssygdom, der nedsætter tåre- og spytkirtelfunktionen. Læs om årsager, symptomer og behandling. Sjögrens syndrom er en kronisk gigtsygdom, som påvirker kroppens kirtelfunktioner, især tåre- og spytkirtler Adult Still's disease is a rare type of inflammatory arthritis that is similar to rheumatoid arthritis. It shares characteristics of systemic-onset juvenile idiopathic arthritis, but it begins in adulthood

Iris Strillinger (48) litt 20 Jahre, ohne zu wissen, woran. Mit 43 bekam sie die Diagnose Morbus Fabry. Im Interview erzählt die Obfrau der Morbus-Fabry-Selbsthilfegruppe Österreich, was es heißt, eine so seltene Krankheit zu haben Today is the day of the rare disease. My name is Morbus Still. The frequency of those affected is estimated at a 1-5 of 10,000 people. An invisible and unpredictable disease affecting the entire body.Symptoms are:Fever bouts up to 40 ° Celsius and that for up to weeks.Joint and muscle pain.In som Definisjon. Sykdommen blant voksne (Adult Stills sykdom, AOSD) skilles fra Stills sykdom hos barn som er identisk med juvenil artritt (barneleddgikt), systemisk type, selv om tilstandene har flere felles kjennetegn.Stills sykdom er både hos barn og voksne preget av daglige episoder med høy feber, periodevis utslett og leddhevelser ()

Adulter Morbus Still SpringerLin

What is Cushing Syndrome? Cushing syndrome describes the signs and symptoms associated with prolonged exposure to inappropriately high levels of the hormone cortisol. The most common cause of this. FPnotebook.com is a rapid access, point-of-care medical reference for primary care and emergency clinicians. Started in 1995, this collection now contains 6664 interlinked topic pages divided into a tree of 31 specialty books and 728 chapters The Korsakoff`s syndrome (also known as Morbus Korsakoff or Amnestic syndrome) is a special form of Amnesia. It was first described by the Russian psychiatrist and neurologist Sergei Korsakoff (1854-1900) in a study about chronic alcoholics in 1887. The disease can be placed under the category of secondary dementia The suggested length of time for high level noise exposure above 70 decibels is 7 to 8 hours. Morbus Meniere Syndrome some people have been known to still experience some sort of hearing loss following that time frame

Reflex Sympathetic Dystrophy Syndrome (RSDS) is relatively common and has been reported to occur after 5% of all traumatic injuries. It may occur following fractures to the extremities, joint sprains or following surgery Morbus Still ili Chauffard-Ramonov sindrom je bolest koja se karakteriše oboljenjem zglobova, pojavom visoke temperature i karakteristične ospe po koži. Epidemiologija: Tačan uzrok nastanka ove bolesti još uvijek nije dovoljno poznat CRPS (Morbus Sudeck) ist die Folge einer Gewebsverletzung. Eine solche Verletzung ensteht häufig, auch durch kleine Unfälle, kann aber auch die Folge operativer Eingriffe sein. Mehrere Wochen nach der Verletzung treten plötzlich starke Schmerzen in der betreffenden Region auf, die durch die ursprüngliche Verletzung nicht mehr zu erklären sind Morbus Still (Still-Syndrom des Erwachsenenalters) Welche Symptome treten auf? 3.9 Seltene rheumatische Erkrankungen • gemeinsam mehr bewegen • Die Rheuma-Liga ist die größte Gemeinschaft und Interessenvertretung rheumakranker Menschen in Deutschland. Wir informieren und beraten fachkompetent und frei von kommerziellen Interessen Dupuytren's contracture is a non-specific affliction but primarily affects: Non-modifiable. People of Scandinavian or Northern European ancestry, it has been called the Viking disease, though it is also widespread in some Mediterranean countries (e.g., Spain and Bosnia) Dupuytren's is unusual among ethnic groups such as Chinese and Africans

In spite of tremendous advances in treating the chronic inflammatory bowel diseases Morbus Crohn and ulcerative colitis with medication, the chronic inflammation still cannot be kept sufficiently. A great deal of hope is being placed in a new generation of medications, biopharmaceuticals, for treatment of still incurable diseases such as certain cancers, Alzheimer's disease and Parkinson's disease With Reverso you can find the German translation, definition or synonym for Morbus-Down-Syndrom and thousands of other words. You can complete the translation of Morbus-Down-Syndrom given by the German-English Collins dictionary with other dictionaries: Wikipedia, Lexilogos, Langenscheidt, Duden, Wissen, Oxford, Collins dictionaries.. Ménière's disease usually starts between the ages of 20 and 50 years; however, it is not uncommon for elderly people to develop the disease without a previous history of symptoms. Ménière's disease affects men and women in equal numbers. In most patients only one ear is affected but in about 15% both ears are involved

Still-Syndrom - DocCheck Flexiko

(OBQ08.183) Lateral tibial physeal stapling is a treatment option for adolescent Blount's disease. How is the staple an example of the Hueter-Volkmann principle? How is the staple an example of the Hueter-Volkmann principle Schüttellähmung Parkinson Syndrom. How To Increase Dopamine Levels In The Brain (NATURAL WAYS) -PART 1- Raise Your Dopamine Naturally - Duration: 6:39. Natural Health Evolution 81,261 view Morbus Bechterew - eller rygsøjlegigt - er en inflammatorisk gigtsygdom, hvor gigtbetændelsen bl.a. sætter sig i ryghvirvlerne. På latin kaldes sygdommen spondylitis ankylopoietica. Spondylitis betyder betændelse i ryghvirvlerne, og ankylopoietica er navnet på en type ledbetændelse, der har tendens til at fremkalde stivhed i leddene

Trotzdem ist es erfreulich, dass die Therapie des Hodgkin-Lymphoms nunmehr überwiegend positiv verläuft. Betrachtet man die sogenannten Cancer-Survivors, also Krebs-Langzeitüberlebende, so sind diese sehr häufig ehemalige Morbus-Hodgkin-PatientInnen. Einfach, weil Morbus Hodgkin sehr gut therapierbar ist Sneddon syndrome (SS) is increasingly recognised as a cause of ischaemic stroke in young adults. As the natural course of SS is not well defined, the authors performed a prospective six year clinical and neuroradiological follow up study. Thirteen patients with definite diagnosis of SS (livedo. 1 Definition. The CRPS is a chronic neurologic disease, which occurs after soft tissue or nerve injury, often in association with the fracture of an extremity.The old term Sudeck's syndrome is still frequently used to describe CRPS of type 1 named after its discoverer Paul Sudeck (1866-1945), a Hamburg-based surgeon Grover's disease is a rare, transient skin disorder that consists of small, firm, raised red lesions, most often on the skin of the chest and back. Diagnosis of this disorder becomes apparent under microscopic examination when the loss of the cement that holds the skin cells together is observed

Ledderhose disease is a type of plantar fibromatosis characterized by the growth of hard and round or flattened nodules (lumps) on the soles of the feet. It is generally seen in middle-aged and elderly people, and occurs in men about 10 times more often than in women Presentation: Symptoms . forefoot pain, swelling and stiffness l ocalized to head of the second MT. worse with weight bearing activities; Physical exam . inspection. peri-articular swellin Gilbert syndrome is diagnosed more often in males than females. The disorder affects approximately 3-7 percent of individuals in the general population. Gilbert syndrome affects individuals of all races. It is present at birth, but may remain undiagnosed until the late teens or early twenties Also known as Hansen's disease; it is a chronic bacterial infection that damages the nerves (especially in the limbs and facial area) and can cause severe skin damage. If left untreated, very serious complications occur including blindness and disfigurement

Still's Disease Causes, Treatment & Prognosis - MedicineNe

  1. In KD (Kennedy's Disease) the nerve cells become dysfunctional and eventually die, leaving the muscles unable to contract. The androgen receptor is a protein that resides inside the nerve cell. Many cells have the androgen receptor protein, but motor neurons have more than most
  2. Publicationdate February 17, 2016 In this article we will discuss the MRI-features used to evaluate Crohn's disease of the small bowel and the colon. A systematic approach is presented to grade disease activity resulting in a simple classification of mild, moderate and severe disease
  3. Crouzon Syndrome Before & After Pictures in Dallas, TX. Here at the International Craniofacial Institute in Dallas, Texas, we have treated many patients with Crouzon syndrome, allowing them to enjoy better brain development and restore facial symmetry and balance
  4. First described by the American dermatologist John T. Bowen in 1912, Bowen disease is a squamous cell carcinoma (SCC) in situ with the potential for significant lateral spread

Bowen's Disease - Bowen Disease - Bowens Disease - Disease, Bowen - Disease, Bowen's : Français: Maladie de Bowen - Dyskératose lenticulaire en disque : Deutsch: Bowen-Krankheit - Bowen-Syndrom - Dermatitis praecancerosa Bowen - Morbus Bowen : Español: Enfermedad de Bowen : Português: Doença de Bowe Wegener's granulomatosis is a very rare disease that affects many different organs and systems of the body. It mainly attacks the respiratory system (sinuses, nose, windpipe, and the lungs) and the kidneys Scheuermann's disease, or Scheuermann's Kyphosis, is a condition in which the normal roundback in the upper spine is increased and results in a hunchback appearance, but rarely causes back pain

Sjögren's is a systemic disease, and its symptoms are felt throughout the entire body. Symptoms vary from person to person but may include: • a dry, gritty or burning sensation in the eye Below is an example of Dupuytren's contracture (Dupuytren's disease, morbus Dupuytren) in an early developmental stage (upper nodule, dotted line) and an initial stage (lower nodule), without contraction of fingers (= stage N). The solid line indicates the area to be exposed in radiation therapy Still's disease is an auto-inflammatory disease that affects both children and adults, and is characterized by high spiking fevers, intermittent rash and arthritis Das Still-Syndrom umfasst zwei Ausprägungen, die systemisch juvenile idiopathische Arthritis (SJIA) und die adulte Form, Adult Onset Still`s Disease (AOSD). SJIA oder Morbus Still ist die.

Adult Still disease: MedlinePlus Medical Encyclopedi

Adult‐onset Still's disease (AOSD) is frequently refractory to standard therapy. Tocilizumab (TCZ) has demonstrated efficacy in single cases and in small series of patients with AOSD. The aim of this multicenter study was to assess the efficacy of TCZ in patients with AOSD refractory to conventional treatment Freiberg's disease affects the long bones of the foot, known as the metatarsals, specifically the second and third. If you are unsure whether this is the specific pain that you are experiencing or if you need treatment for Freiberg's disease, here are a few things to put on your checklist that will suggest if this is the case, or not How to Diagnose and Treat Crohn's Disease. Crohn's disease, a type of inflammatory bowel disease (IBD), is a condition in which the lining of your digestive tract becomes inflamed, causing severe diarrhea and abdominal pain. The..

Adult-onset Still disease Radiology Reference Article

  1. Familial Scheuermann disease is characterized by kyphotic deformity of the spine that develops in adolescence. The spinal deformity includes irregularities of the vertebral endplates, the presence of Schmorl's nodes, disk-space narrowing, and vertebral wedging and is diagnosed using lateral radiographs of the spine
  2. About Loeffler's Syndrome: Simple pulmonary eosinophilia is characterized by abnormal chest X-ray findings. These vary -- the abnormality may appear in one part of the lung at one time, but the next X-ray may show no pathology or a problem in a different part of the lung
  3. A SUCCESSFUL NEW APPROACH TO MENIERE'S DISEASE - The John of Ohio Meniere's Regimen - Updated - June 2014 NOTE: Changes in this version of the regimen, compared to previous ones, include removal of references to Vertigoheel and Cocculus Compositum, which are no longer available in the US. Course of the Disease
  4. Cushing's Disease vs. Cushing's Syndrome. Cushing's disease is not the same as Cushing's syndrome. Cushing's syndrome refers to the general state characterized by excessive levels of cortisol in the blood. Elevated cortisol levels can occur for reasons other than a pituitary tumor, including: Tumors of the adrenal glands producing cortiso
  5. The Moebius Syndrome Foundation's mission is to provide information and support to individuals with Moebius syndrome and their families, promote greater awareness and understanding of Moebius syndrome, and to advocate for scientific research to advance the diagnosis and treatment of Moebius syndrome and its associated conditions
  6. Stickler syndrome affects connective tissue throughout the body, but most notably in the eyes (it is the most common cause of retinal detachment in children), ears, face, and joints. Stickler syndrome affects 1 out of every 7,500 people, but experts believe that it is widely under-diagnosed
  7. Addison's disease occurs when the adrenal cortex is damaged and the adrenal glands do not produce enough steroid hormones called cortisol and aldosterone. Cortisol regulates the body's reaction to.


Sweet's syndrome (also known as acute febrile neutrophilic dermatosis) is a rare skin disorder characterised by a fever and the appearance of tender red or purple lumps or patches on the skin that may ulcerate Raynaud's disease is a rare disorder of the blood vessels, usually in the fingers and toes. It causes the blood vessels to narrow when you are cold or feeling stressed. When this happens, blood can't get to the surface of the skin and the affected areas turn white and blue. When the blood flow returns, the skin turns red and throbs or tingles Paget's disease of the nipple is a rare form of breast cancer in which cancer cells collect in or around the nipple. The cancer usually affects the ducts of the nipple first, then spreads to the nipple surface and the areola. Learn more about Paget's disease of the nipple

Adult-Onset Still's Disease - WebM

Bright's disease is an obsolete classification for nephritis, a kidney condition. It was named after Dr. Richard Bright, who described the condition in the early 19th century. A lack of understanding of how the kidneys work at the time meant that the conditions now known as chronic and acute nephritis were both considered Bright's disease Morbus is not intended to validate anyone's experiences over other's but rather to acknowledge the spectrum of health and ability that exists between the polarised states of able and disabled, normal and abnormal, well and unwell. It is my hope that by drawing attention to concepts of body occupancy, ethics, repair, and the physica Stargardt disease (STGD) is the most common childhood recessively inherited macular dystrophy. The condition has a genetic basis due to mutations in the ABCA4 gene, and results from the accumulation of visual cycle kinetics-derived byproducts in the retinal pigmented epithelium (RPE) with secondary photoreceptor dysfunction and death Bowen's disease is a type of skin cancer, find out more about getting diagnosed and what treatment you might expect. Bowen's disease is a very early form of squamous cell skin cancer. It's also called squamous cell carcinoma in situ. Doctors call Bowen's disease pre invasive. That means that.

Stills sjukdom - Wikipedi

  1. This page was last edited on 19 June 2018, at 00:23. Files are available under licenses specified on their description page. All structured data from the file and property namespaces is available under the Creative Commons CC0 License; all unstructured text is available under the Creative Commons Attribution-ShareAlike License; additional terms may apply
  2. Bowen's disease is a very early form of skin cancer that's easily treatable. The main sign is a red, scaly patch on the skin. It affects the squamous cells - which are in the outermost layer of skin - and is sometimes referred to as squamous cell carcinoma in situ. The patch is usually.
  3. Complex regional pain syndrome (CRPS), also known as Morbus Sudeck, is characterised by disinhibition of various sensory and motor areas in the brain. A multidisciplinary research group has now.

Adulter Morbus Still, Schnitzler-Syndrom und

  1. Reiter's syndrome: Introduction. Reiter's syndrome is a rare type of arthritis that causes inflammation of the urinary tract, eyes, skin, mucus membranes, and joints. . Reiter's syndrome, also called reactive arthritis, is believed to occur as a reaction to certain infections of the reproductive system and the digestiv
  2. Roman medical writers (and the Greeks before them) had quite vast and in-depth knowledge of the diseases that plagued their populations. Still, they were pretty clueless about the actual methods of transmission of infectious diseases (like malaria) and had a very hard time distinguishing among the various kinds of pox
  3. en A pharmaceutical preparation is disclosed for the prevention, treatment and relief from the consequences of alcohol abuse, viral hepatitis, steatohepatitis, acute and chronic pancreatitis, Alzheimer's disease, Parkinson's disease, toxic kidney diseases, acute kidney failure, toxic side effects on dosage of chemotherapeutics, diabetes.
  4. Acute febrile neutrophilic dermatosis, also termed Sweet syndrome, is a reactive process characterized by the abrupt onset of tender, red-to-purple papules, and nodules that coalesce to form plaques. The plaques usually occur on the upper extremities, face, or neck and are typically accompanied by fever and peripheral neutrophilia
  5. g intestinal neural plexus; in Hirschsprung, usually are heterogeneous defects in genes regulating migration and survival of neuroblasts (endothelin 3 and its receptor, OMIM 600155), glial cell derived growth factor (neurogenesis) and receptor tyrosine kinase activity (RET, Ann Med 2006;38:11, Am J.
  6. Still, against popular belief, most children with Down's syndrome are born to young mothers: 51 % to mothers under 30, 72 % to women under 35. The deviation is registered in all races and affects both sexes. The term mongolism comes from the upward slanting eyes which give the impression of an oriental person
  7. Gilbert's syndrome (GS) is a common hyperbilirubinaemia syndrome caused by reduced conjugation of serum bilirubin by the liver. Although it is considered as a common and harmless condition not requiring treatment symptoms associated with GS may be unfavorable

Adiposis dolorosa is a condition characterized by painful folds of fatty (adipose) tissue or the growth of multiple noncancerous (benign) fatty tumors called lipomas. This condition occurs most often in women who are overweight or obese, and signs and symptoms typically appear between ages 35 and 50 Crouzon syndrome is a disorder that is genetic. In the United States it is estimated that approximately 1 for every 60,000 live births has Crouzon syndrome. It affects babies of every ethnic background. It is believed to be inherited but it could possibly be spontaneous Sjögren syndrome is the third most common rheumatic disorder, after rheumatoid arthritis and systemic lupus erythematosus Systemic autoimmune disease that presents typically with xerostomia (dry mouth), keratoconjunctivitis sicca (dry eyes), rheumatoid arthritis and hypergammaglobulinemi Sever's disease, also called calcaneal apophysitis is an overuse injury and is a common cause of pain at the back of the heel in the skeletally immature children aged 8 to 15 years Gorham's (GOR-amz) disease is a very rare skeletal condition of uncertain etiology, characterized by the uncontrolled proliferation of distended, thin-walled vascular or lymphatic channels within bone, which leads to resorption and replacement of bone with angiomas and/or fibrosis.1, 2 Because of the loss of the affected bone, the condition has been referred to as disappearing bone disease. disease, impairment of the normal state or functioning of the body as a whole or of any of its parts. Some diseases are acute, producing severe symptoms that terminate after a short time, e.g., pneumonia; others are chronic disorders, e.g., arthritis, that last a long time; and still others return periodically and are termed recurrent, e.g., malaria