| SG | Sachs-Georgi [test]; salivary gland; serum globulin; serum glucose; signs; skin graft; soluble gelat... |
|---|---|
| SGR | Sachs-Georgi reaction; Shwartzman generalized reaction; skin galvanic reflex; submandibular gland re... |
| SHEENT | skin, head, eyes, ears, nose, and throat |
| Sk | skin |
| SKALP | skin-derived antileukoproteinase |
| 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) |
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| Caffey-Kempe syndrome | <radiology> Multiple assymetrical fractures, separation of distal epiphyses, irregularity and fragmentation of metaphyses, bucket-handle fracture, corner fracture of elbow, knee, ankle (sudden twisting motion), isolated spiral fracture, extensive periosteal reaction (subperiosteal haemorrhage), exuberant callus formation, cortical hyperostosis extending to epiphyseal plate, avulsion fracture at ligamentous insertion, subdural haematoma (most common), brain atrophy (up to 100%), infarction (50%), subdural hygroma, encephalomalacia, porencephaly (12 Dec 1998) |
| Caffey-Silverman syndrome | Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood. Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome. (05 Mar 2000) |
| Caffey's syndrome | Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood. Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome. (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) |
| cardiofacial syndrome | <syndrome> Transient or persistent unilateral partial lower facial paresis accompanying some congenital heart disease. A group of syndromes characterised by congenital cardiovascular, bone, soft tissue, and facial abnormalities. Examples include Rubinstein-Taybi syndrome, Noonan's syndrome and Williams' syndrome. Synonym: Williams' syndrome. (05 Mar 2000) |