| LGS | Langer-Giedion syndrome; Lennox-Gastaut syndrome; limb girdle syndrome |
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| MPS | meconium plug syndrome; medial premotor system; Member of the Pharmaceutical Society; microbial prof... |
| NBS | N-bromosuccinimide; National Bureau of Standards; neuroblastoma supressor; nevoid basal cell carcino... |
| PES | Patient Escort Service; photoelectron spectroscopy; physicians' equity services; polyethylene sulfon... |
| PSS | painful shoulder syndrome; physiologic saline solution; porcine stress syndrome; primary Sjogren syn... |
| Burnett's syndrome | <syndrome> A form of metabolic acidosis that can result from the excessive consumption of milk (calcium) and antacids (sodium bicarbonate) over a prolonged period of time. This can result in calcium deposits in the kidneys and body tissues. Symptoms include nausea, vomiting and weakness. May be seen as a complication of peptic ulcer therapy. (27 Sep 1997) |
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| burning foot syndrome | <syndrome> A disorder observed in prisoners-of-war in World War II, now believed to be due to a pantothenate deficiency. (05 Mar 2000) |
| burning mouth syndrome | <syndrome> A group of painful oral symptoms associated with a burning or similar sensation. There is usually a significant organic component with a degree of functional overlay; it is not limited to the psychophysiologic group of disorders. (12 Dec 1998) |
| burning vulva syndrome | <syndrome> Persistent vulvodynia in which a physical cause has not been identified. (05 Mar 2000) |
| Buschke-Ollendorf syndrome | Osteopoikilosis with skin lesions, most commonly small elastic fibrous nodules on the posterior aspects of the thighs and buttocks; irregular autosomal dominant inheritance. Synonym: Buschke-Ollendorf syndrome. Origin: osteo-+ G. Derma, skin, + poikilos, dappled, + -osis, condition (05 Mar 2000) |
| camptomelic syndrome | <syndrome> Also associated with flat facies, short vertebrae, hypoplastic scapula, and bowed tibia. Synonym: osteochondrodysplasia. (05 Mar 2000) |
| cantrell syndrome | <radiology> Herniation of gut into pericardial sac, common anterior communication in diaphragm and pericardium, associated with congenital defects of sternum, heart, mesentery, anterior abdominal wall, must be excluded in presence of omphalocele, ** diaphragmatic hernia (12 Dec 1998) |
| capgras syndrome | <syndrome> A psychotic disorder characterised by the patient's conviction that certain important or familiar persons in his environment are not real but are "doubles" of themselves or imposters. (12 Dec 1998) |
| Capgras' syndrome | <syndrome> The delusional belief that a person (or persons) close to the schizophrenic patient has been substituted for by one or more impostors; may have an organic aetiology. Synonym: Capgras' phenomenon, illusion of doubles. (05 Mar 2000) |
| capillary leak syndrome | <syndrome> Extravasation of plasma fluid and proteins into the extravascular space, resulting in sometimes fatal hypotension and reduced oxygen perfusion. Clinical capillary leak syndrome is observed in patients who demonstrate a state of generalised leaky capillaries following shock syndromes, low-flow states, ischemia-reperfusion injuries, toxaemias, or poisoning. It can lead to generalised oedema and multiple organ failure., reperfusion injuries and clinical capillary leak syndrome. (12 Dec 1998) |
| caplan's syndrome | <syndrome> Pneumoconiosis associated with rheumatoid arthritis. (12 Dec 1998) |
| caplan syndrome | <radiology> Combination of: necrobiotic rheumatoid lung nodules, coal worker's pneumoconiosis Findings: round, peripheral nodules (0.5 - 5.0 cm), with or without cavitation, nodules associated with subcutaneous rheumatoid nodules (12 Dec 1998) |
| carbohydrate-deficient glycoprotein syndrome | <syndrome> An inborn error of carbohydrate metabolism manifesting as a genetic multisystem disorder of autosomal recessive inheritance. A predominant feature is severe central and peripheral nervous system involvement resulting in psychomotor retardation, seizures, cerebellar ataxia, and other symptoms which include growth retardation, retinitis pigmentosa, hypothyroidism, and fatty liver. The notable biochemical feature is the deficiency of a large number of blood glycoproteins and decreased activities of various blood coagulation factors. (12 Dec 1998) |
| carbonic anhydrase II deficiency syndrome | <syndrome> An inherited deficiency of carbonic anhydrase II that results in osteopetrosis and metabolic acidosis. Synonym: osteopetrosis with renal tubular acidosis. (05 Mar 2000) |
| carcinoid syndrome | <oncology, syndrome> A constellation of symptoms associated with a serotonin-secreting neoplasm known as carcinoid tumour. These tumours may grow anywhere in the gastrointestinal tract (and in the lungs) with approximately 90% in the appendix. The remainder occur in the ileum, stomach, colon or rectum. Symptoms include flushing, rapid pulse, facial swelling, swelling around the eyes, low blood pressure, abdominal pain, weight loss and diarrhoea. (19 Jan 1998) |