| IHH | idiopathic hypogonadotropic hypogonadism; idiopathic hypothalamic hypogonadism; infectious human hep... |
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| IHP | idiopathic hypoparathyroidism; idiopathic hypopituitarism; individualized health plan; inositol hexa... |
| IIP | idiopathic interstitial pneumonia; idiopathic intestinal pseudo-obstruction; increased intracranial ... |
| ILS | idiopathic leucine sensitivity; idiopathic lymphadenopathy syndrome; increase in life span; infrared... |
| IPD | idiopathic Parkinson disease; idiopathic protracted diarrhea; immediate pigment darkening; increase ... |
| purpura urticans | Purpura simplex accompanied by an urticarial eruption. (05 Mar 2000) |
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| hyperglobulinaemic purpura | <haematology> A condition characterised by proliferation of cells resembling lymphocytes or plasma cells in the bone marrow, anaemia, increased sedimentation rate and hyperglobulinaemia. Physical findings include mucosal bleeding, skin purpura and enlargement of the lymph nodes, liver and spleen. Origin: Gr. Haima = blood (27 Sep 1997) |
| hyperglobulinemic purpura | A condition characterised by proliferation of cells resembling lymphocytes or plasma cells in the bone marrow, anaemia, increased sedimentation rate and hyperglobulinaemia. Physical findings include mucosal bleeding, skin purpura and enlargement of the lymph nodes, liver and spleen. (27 Sep 1997) |
| nonthrombocytopenic purpura | The eruption of petechiae or larger ecchymoses, usually unaccompanied by constitutional symptoms and not associated with systemic illness. Synonym: nonthrombocytopenic purpura. (05 Mar 2000) |
| immune thrombocytopenic purpura | <haematology> A low number of platelets in the blood, which is common in people with HIV, but often resolves as immune deficiency worsens. HIV-related ITP usually does not have serious consequences. Its cause has not been definitely determined. Treatment with AZT frequently alleviates the condition. (09 Oct 1997) |
| thrombocytopenia purpura | <haematology> In severe thrombocytopenia, bleeding into skin leads to small petechial haemorrhages. Primary thrombocytopenia purpura is of unknown cause but results from an autoimmune mechanism that causes platelet destruction. Secondary thrombocytopenic purpura may result from drug-induced type II hypersensitivity in which platelets coated with antibody to the drug (which is acting as a hapten) are destroyed in a complement mediated reaction. It can also follow a viral upper respiratory infection and may be seen in association with lupus. (15 Oct 1997) |
| thrombocytopenic purpura | See: idiopathic thrombocytopenic purpura. (05 Mar 2000) |
| thrombopenic purpura | idiopathic thrombocytopenia purpura |
| thrombotic thrombocytopenic purpura | A rapidly fatal or occasionally protracted disease with varied symptoms in addition to purpura, including signs of central nervous system involvement, due to formation of fibrin or platelet thrombi in arterioles and capillaries in many organs. Synonym: Moschcowitz' disease. (05 Mar 2000) |
| equine nonthrombocytopenic purpura | <veterinary> An immune-mediated vasculitis of horses due to immune complex deposition, characteristically as a sequela of strangles. (05 Mar 2000) |
| factitious purpura | Self-induced, often painful, ecchymoses. (05 Mar 2000) |
| fibrinolytic purpura | Purpura in which the bleeding is associated with rapid fibrinolysis of the clot. (05 Mar 2000) |
| acute idiopathic polyneuritis | <neurology, syndrome> Acute infective polyneuritis that results in a form of peripheral neuropathy with temporary loss of movement and sensation due to inflammation of multiple nerves and loss of myelin. The exact cause is unknown but has been associated with an abnormal immune response to viral infection, particularly cytomegalovirus infection, in which there is cell-mediated immunity to a component of myelin. The disease may be autoimmune in origin and complete recovery can take up to six months. Synonym: Guillain-Barre syndrome (12 Jul 2000) |
| chronic idiopathic jaundice | <syndrome> An inherited disorder (autosomal recessive) that is characterised by long-standing mild jaundice. This occurs secondary to an abnormality in the transport of bilirubin from the liver to the biliary system. This leads to an accumulation of bilirubin in the liver. Avoidance of alcohol and medications which can affect the liver is important. Inheritance: autosomal recessive. (27 Sep 1997) |
| chronic idiopathic xanthomatosis | Vague or indefinite term for inherited abnormalities of lipid metabolism leading to xanthoma formation (e.g., primary familial xanthomatosis). (05 Mar 2000) |