| APH | alcohol-positive history; alternative pathway hemolysis; aminoglycoside phosphotransferase; antepart... |
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| APL | abductor pollicis longus; accelerated painless labor; acute promyelocytic leukemia; animal placenta ... |
| APR | abdominoperineal resection; absolute proximal reabsorption; acute phase reaction or reactant; amebic... |
| CPD | calcium pyrophosphate deposition; cephalopelvic disproportion; cerebelloparenchymal disorder; childh... |
| HP | halogen phosphorus; handicapped person; haptoglobin; hard palate; Harvard pump; health profession(al... |
| pituitary myxoedema | Myxoedema resulting from inadequate secretion of the thyrotropic hormone; commonly occurs in association with inadequate secretion of other anterior pituitary hormones. (05 Mar 2000) |
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| pituitary stalk section | Transection of the neurovascular connection between the hypothalamus and the pituitary gland. (05 Mar 2000) |
| posterior pituitary | The cleaned, dried, and powdered posterior lobe obtained from the pituitary body of domestic animals used for food by humans; an oxytocic, vasoconstrictor, antidiuretic, and a stimulant of intestinal motility. Synonym: desiccated pituitary, hypophysis sicca. (05 Mar 2000) |
| postpartum pituitary necrosis syndrome | <syndrome> Hypopituitarism arising from a severe circulatory collapse postpartum, with resultant pituitary necrosis. Synonym: postpartum pituitary necrosis syndrome, thyrohypophysial syndrome. (05 Mar 2000) |
| Cushing's pituitary basophilism | <disease> An increased concentration of glucocorticoid hormone in the bloodstream (produced by the adrenal gland) secondary to a pituitary tumour that is secreting the hormone adrenocorticotropic hormone (ACTH). ACTH serves to stimulate the adrenal gland to produce excess glucocorticoids. (27 Sep 1997) |
| hyaline bodies of pituitary | Accumulations of a gelatinous neurosecretory substance in the axons of the hypothalamohypophyseal tract in the posterior lobe of the hypophysis. (05 Mar 2000) |
| desiccated pituitary | The cleaned, dried, and powdered posterior lobe obtained from the pituitary body of domestic animals used for food by humans; an oxytocic, vasoconstrictor, antidiuretic, and a stimulant of intestinal motility. Synonym: desiccated pituitary, hypophysis sicca. (05 Mar 2000) |
| dwarfism, pituitary | A form of dwarfism due to absence or hypofunction of the anterior pituitary gland. (12 Dec 1998) |
| enlarged pituitary infundibulum | <radiology> Histiocytosis X, eosinophilic granuloma, Hand-Schuller-Christian disease, Letterer-Siwe disease, sarcoidosis (12 Dec 1998) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |
| adult lactase deficiency | Onset of lactase deficiency, with resulting milk intolerance and malabsorption, in adulthood. Inherited forms may not be manifested until adulthood; any process that damages the intestinal lining cells can cause lactase deficiency in adults. (05 Mar 2000) |
| alpha-1 antitrypsin deficiency | <chest medicine> Deficiency of the protease inhibitor alpha-1 antitrypsin, leads primarily to degradation of elastin of the alveolar walls, as well as other structural proteins of a variety of tissues. The lack of this protein leads to damage of various organs, but mainly to the lung and liver. symptoms may become apparent at a very early age or in adulthood, manifesting either as shortness of breath or liver related symptoms (jaundice, fatigue, fluid in the abdomen, mental changes, or gastrointestinal bleeding). There are several options for treatment of the lung disease, including replacement of the missing protein. Treatment of the liver disease is a well-timed liver transplant (12 Dec 1998) |
| alpha-1-proteinase deficiency | Absence of a serum proteinase inhibitor that may cause nodular non-suppurative panniculitis. (05 Mar 2000) |
| alpha-antitrypsin deficiency | <enzyme> A specific enzyme (alpha 1 antitrypsinase) that when absent genetically can result in panacinar emphysema (lung disease) and liver disease. There is no specific treatment for this condition other than supportive care for the liver and lung complications. Medications such as alpha-1proteinase inhibitor is given regularly to these patients. Incidence: approximately 1 in 10,000. (02 Jan 1998) |
| anaemia, iron deficiency | Deficiency of iron results in anaemia because iron is necessary to make haemoglobin, the key molecule in red blood cells responsible for the transport of oxygen. In iron deficiency anaemia, the red cells are unusally small (microcytic) and pale (hypochromic). Characteristic features of iron deficiency anaemia in children include failure to thrive (grow) and increased infections. The treatment of iron deficiency anaemia, whether it be in children or adults, is with iron and iron-containing foods. Food sources of iron include meat, poultry, eggs, vegetables and cereals (especially those fortified with iron). According to the National Academy of Sciences, the Recommended Dietary Allowances of iron are 15 milligrams per day for women and 10 milligrams per day for men. Anaemia characterised by low or absent iron stores, low serum iron concentration, elevated free erythrocyte porphorin, low transferrin saturation, elevated transferrin, low serum ferritin, low haemoglobin concentration or haematocrit, and hypochromic microcytic red blood cells. Symptoms may include pallor, angular stomatitis and other oral lesions, gastrointestinal complaints, retinal haemorrhages and exudates, and thinning and brittleness of the nails. Among the causes of iron-deficiency anaemia are inadequate iron intake, impaired iron absorption, increased blood loss and increased requirements such as infancy, pregnancy, and lactation. (12 Dec 1998) |