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Adverse effects with these treatments were common, with 50–60% of those being treated experiencing flu-like symptoms and nearly a third experiencing depression or other emotional issues. [16] Treatment during the first six months of infection (the acute stage) is more effective than when hepatitis C has entered the chronic stage. [27]
A child with Hand-Schüller-Christian Disease: Specialty: Dermatology: Symptoms: Triad of bulging eyes, breakdown of bone, diabetes insipidus [1] Other symptoms eg. bone pain, facial asymmetry, ear infections, teeth/gum problems, liver and lung disease signs. [1] [2] Usual onset: Age 2-6 [2] Causes: Genetic mutation in the MAPKinase pathway [1 ...
The response to treatment is similar to that in adults. [10] It shows a similar dependence on the genotype. Recurrence after transplant is universal and the outcomes after transplant are usually poor. [11] In children treatment should be initiated within 12 weeks of the detection of the viral RNA if viral clearance has not occurred within this ...
Integrated Management of Childhood Illness (IMCI) is a systematic approach to children's health which focuses on the whole child. [citation needed] This means focusing not only on curative care but also on prevention of disease. The approach was developed by United Nations Children's Fund and the World Health Organization in 1995. [1]
Chronic diseases in children may have a genetic (hereditary) cause, an environmental (acquired) cause or a combination of both. Early identification and treatment of the disease is key to successful health outcomes. Chronic diseases can affect multiple organ systems and can, therefore, manifest in different ways.
Common causes for acute liver failure are paracetamol (acetaminophen) overdose, idiosyncratic reaction to medication (e.g. tetracycline, troglitazone), excessive alcohol consumption (severe alcoholic hepatitis), viral hepatitis (hepatitis A or B—it is extremely uncommon in hepatitis C), acute fatty liver of pregnancy, and idiopathic (without ...
Older children or adults generally present with a wide range of signs and symptoms that overlap with other disorders. [5] They may have diarrhoea, stomach pain, vomiting, or poor growth, a sign of malabsorption. They may have signs of bile duct problems, like itchiness, jaundice, pale stool, or dark urine. Their feces may be excessively greasy.
Inborn errors of metabolism are often referred to as congenital metabolic diseases or inherited metabolic disorders. [2] Another term used to describe these disorders is "enzymopathies". This term was created following the study of biodynamic enzymology , a science based on the study of the enzymes and their products.