| PNS | paraneoplastic syndrome; parasympathetic nervous system; partial nonprogressive stroke; peripheral n... |
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| MEDAC Syndrome | Multiple-Endocrine Deficiency Autoimmune-Candidiasis |
| AEP | acute edematous pancreatitis; artificial endocrine pancreas; auditory evoked potential; average evok... |
| AES | acetone-extracted serum; American Electroencephalographic Society; American Encephalographic Society... |
| EC | effective concentration; ejection click; electrochemical; electron capture; embryonal carcinoma; eme... |
| myofascial pain syndromes | Muscular pain in numerous body regions that can be reproduced by pressure on trigger points, localised hardenings in skeletal muscle tissue. Pain is referred to a location distant from the trigger points. A prime example is the temporomandibular joint dysfunction syndrome. (12 Dec 1998) |
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| postgastrectomy syndromes | Sequelae of gastrectomy from the second week after operation on. Include recurrent or anastomotic ulcer, postprandial syndromes (dumping syndrome and late postprandial hypoglycaemia), disordered bowel action, and nutritional deficiencies. (12 Dec 1998) |
| pre-excitation syndromes | Conditions characterised by activation of the whole or some part of the ventricle by the atrial impulse earlier than would be expected if the impulse reached the ventricle by way of the normal specific conduction system only. (12 Dec 1998) |
| sleep apnea syndromes | Disorders involving apneic episodes during sleep. They may be due to cessation of diaphragmatic movement, obstruction of upper airway air flow, or a combination of these, and may be associated with hypersomnolence, insomnia, or obesity. (12 Dec 1998) |
| neoplastic syndromes, hereditary | The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumour tends to occur at an earlier than average age, individuals may have more than one primary tumour, the tumours may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance. (12 Dec 1998) |
| nerve compression syndromes | Repeated or prolonged pressure on a nerve root or peripheral nerve leading to ischemia, the response to which is oedema above and below the source of pressure. If the pressure is not relieved, fibrosis tends to develop. Types of nerve compression syndromes are the neuropathy caused by intervertebral disk herniation, compression of the median nerve in the carpal tunnel, compression of the ulnar nerve in the elbow, and compression of the lateral cutaneous nerve of the thigh in meralgia paresthetica. This is also called pressure neuropathy. (12 Dec 1998) |
| syndromes of paranasal sinuses | <radiology> Gardner: osteomas, Kartagener: chronic infection, basal cell-nevoid, neurofibromatosis, Down (trisomy 21): hypoplastic frontal, sphenoid, with or without ethmoid, progeria: absent frontal sinuses; dwarf, immature, cleidocranial dysostosis: all sinuses absent/small (12 Dec 1998) |
| dry eye syndromes | Corneal and conjunctival dryness due to deficient tear production, predominantly in menopausal and post-menopausal women. Filamentary keratitis or erosion of the conjunctival and corneal epithelium may be caused by these disorders. Sensation of the presence of a foreign body in the eye and burning of the eyes may occur. (12 Dec 1998) |
| immunologic deficiency syndromes | Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. (12 Dec 1998) |
| overgrowth syndromes | Conditions with multiple abnormalities including excessive growth. Early overgrowth syndromes that affecting children include the fragile x and beckwith-wiedemannn syndromes. Overactivity of the pituitary gland with overproductiuon of growth hormone causes overgrowth before adolescence and a distinctive pattern of overgrowth called acromegaly. (12 Dec 1998) |
| euthyroid sick syndromes | Abnormalities in thyroid hormone and thyroid-stimulating hormone levels, often simulating hypothyroidism, in euthyroid patients suffering some other illness, such as diabetes mellitus or liver cirrhosis. (12 Dec 1998) |
| bone diseases, endocrine | Diseases of the bones related to hyperfunction or hypofunction of the endocrine glands. (12 Dec 1998) |
| multiple endocrine adenomatosis | The presence of functioning tumours in more than one endocrine gland, commonly the pancreatic islets and parathyroid glands, which may be associated with Zollinger-Ellison syndrome; dominant inheritance. Synonym: multiple endocrine adenomatosis. (05 Mar 2000) |
| multiple endocrine deficiency syndrome | <syndrome> Acquired deficiency of the function of several endocrine glands, usually on an auto-immune basis. Synonym: multiple glandular deficiency syndrome. (05 Mar 2000) |
| multiple endocrine neoplasia | (type I) This is a hereditary disorder in which two or more of the following glands: parathyroid, pancreas, pituitary, adrenals or thyroid develop hyperplasia or a tumour. (type II) This is a hereditary disorder in which two or more of the following glands: thyroid, adrenal or parathyroid, develop overgrowth (hyperplasia) or malignant cells (cancer). The underlying cause is genetic and a positive family history for this illness is a risk factor. Incidence: approximately 3 in 100,000 people in the general population. Origin: Gr. Plassein = to form (27 Sep 1997) |