| IHD | Ischemic Heart Disease = Coronary Heart(Artery) Disease = Atheroscler... |
|---|---|
| LCP Disease | Legg-Calve-Perthes Disease ? Stages of LCP Disease(= Juvenile Idiopathic AVN) &nb... |
| AID | acquired immunodeficiency disease; acute infectious disease; acute ionization detector; Agency for I... |
| BD | barbital-dependent; barbiturate dependence; base deficit; base of prism down; basophilic degeneratio... |
| CAD | cadaver, cadaveric; cold agglutinin disease; compressed air disease; computer-assisted design; compu... |
| Korff, Karl von | <person> 20th century German anatomist and histologist. See: Korff's fibres. (05 Mar 2000) |
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| Kupffer, Karl Wilhelm von | <person> B. Munich, Nov. 14th, 1829. Was an Anatomist and Embryologist. Was Professor of Anatomy in Kiel (1867), in Konigsberg (1875) and in Munich (1880). D. Munich, 1902. Kupffer's Cells - "stellate cells" in the lining of blood channels in the liver. Lived: 1829-1902. (05 Dec 1998) |
| Langenbeck, Bernhard von | <person> German surgeon, 1810-1887. See: Langenbeck's triangle. (05 Mar 2000) |
| Fraunhofer, Joseph von | <person> German optician, 1787-1826. See: Fraunhofer's lines. (05 Mar 2000) |
| Frerichs, Friedrich von | <person> German pathologist and clinician, 1819-1885. See: Frerichs' theory. (05 Mar 2000) |
| Frey, Max von | <person> German physician, 1852-1932. See: Frey's hairs. (05 Mar 2000) |
| Lenhossek, Michael von | <person> Hungarian anatomist, 1863-1937. See: Lenhossek's processes. (05 Mar 2000) |
| Leydig, Franz von | <person> In 1855 was appointed Professor of Histology in Wurzburg and later in Tubingen and Bonn. Was the founder of Comparative Histology. Leydig's Cells - interstitial cells of the testis. Lived: 1821-1908. B. Rothenburg, May 21st, 1821, d. Apr 13th, 1908. (05 Dec 1998) |
| Liebermann, Leo von | <person> Hungarian physician, 1852-1926. See: Burchard-Liebermann reaction, Liebermann-Burchard test. (05 Mar 2000) |
| Liebermeister, Carl von | <person> German physician, 1833-1901. See: Liebermeister's rule. (05 Mar 2000) |
| Liebig, Baron Justus von | <person> German chemist, 1803-1873. See: Liebig's theory. (05 Mar 2000) |
| lindau-von hippel syndrome | <syndrome> The cardinal features of what is more commonly called von hippel-lindau (vhl) syndrome are benign blood-vessel tumours that most typically affect the eye and the brain. The eye tumours are termed angiomata and are in the retina. The brain tumours are termed haemangioblastoma and are in the cerebellum. Vhl is complex. There can also be blood-vessel tumours (haemangiomata) in the spinal cord, adrenal glands, liver, and lungs. Pheochromocytoma (a benign tumour of adrenal-like tissue) occurs in some patients. The combination of high blood pressure (hypertension) with angioma may cause bleeding under the skull (subarachnoid haemorrhage). Kidney tumours (like hypernephromas) may be malignant and metastasize. An abnormal elevation of red blood cells (polycythemia) can be due to the haemangioblastoma of the cerebellum or the hypernephroma. Multiple cysts can occur in the pancreas and kidneys. Patients with kidney problems or pancreatic cysts do not have pheochromocytoma, and visa versa. Lab findings in vhl may include high calcium (hypercalcaemia) and low potassium (hypokalaemia) occurring with the pheochromocytoma. Vhl is inherited as an autosomal dominant trait. The gene on one of the non-sex chromosomes is dominant over the normal gene with which it is paired so that one vhl gene is sufficient to cause the vhl syndrome. If a person has vhl, the chance for each of their children to receive the vhl gene is one-half (50%). The vhl gene has been mapped to chromosome 3 (the 3rd volume in the book of life) in region 3p26-p25. The vhl gene has the characteristics of a tumour-suppressor gene. The person with vhl inherits one inactive copy of the vhl gene (a germline mutation) from one of their parents. But the normal gene with which it is paired is still enough to suppress the formation of a tumour. Then, in one cell in the vhl patient's body, another mutation (a somatic mutation) occurs, inactivating the other vhl gene. Thus, both copies of the vhl gene are inactivated and a tumour arises in the vhl patient. The syndrome is named for the german ophthalmologist eugen von hippel who described the charcteristic eye blood-vessel tumours in 1904 and the swedish pathologist arvid lindau who recognised the association between the eye tumours and the blood-vessel tumours of the cerebellum and other parts of the central nervous system in 1926-7. (12 Dec 1998) |
| Ludwig, Wilhelm Friedrich von | <person> German surgeon, 1790-1865. See: Ludwig's angina. (05 Mar 2000) |
| aaa disease | Endemic anaemia of ancient Egypt, ascribed in the Papyrus Ebers to intestinal infestation with ancylostoma; now called ancylostomiasis. (05 Mar 2000) |
| ABO haemolytic disease of the newborn | Erythroblastosis foetalis due to maternal-foetal incompatibility with respect to an antigen of the ABO blood group; the foetus possesses A or B antigen which is lacking in the mother, and the mother produces immune antibody which causes haemolysis of foetal erythrocytes. (05 Mar 2000) |