| JA | judgment analysis; juvenile atrophy; juxta-articular |
|---|---|
| LCCA | late cortical cerebellar atrophy; leukoclastic angiitis |
| LOA | leave of absence; Leber optic atrophy; left occipitoanterior [fetal position] |
| MSA | major serologic antigen; male-specific antigen; mannitol salt agar; Medical Services Administration;... |
| NMA | National Malaria Association; National Medical Association; neurogenic muscular atrophy; N-nitroso-N... |
| familial spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
|---|---|
| Kienbock's atrophy | Acute atrophy of bone in an extremity following inflammation. (05 Mar 2000) |
| fatty atrophy | Fatty infiltration secondary to an atrophy of the essential elements of an organ or tissue. (05 Mar 2000) |
| Zimmerlin's atrophy | A variety of hereditary progressive muscular atrophy in which the atrophy begins in the upper half of the body. (05 Mar 2000) |
| Leber's hereditary optic atrophy | Hereditary degeneration of the optic nerve and papillomacular bundle with resulting rapid loss of central vision, progressive for several weeks, then usually stationary with permanent central scotoma; age of onset is variable, most often in the third decade; more males than females are affected and transmission is cytoplasmic and strictly on the female side. Mutation on the mitochondrial chromosome involved, which presumably interacts with an X-linked mutant. This mechanism may explain the bizarre sex ratio, which differs significantly from one country to another. (05 Mar 2000) |
| linear atrophy | Bands of thin wrinkled skin, initially red but becoming purple and white, which occur commonly on the abdomen, buttocks, and thighs at puberty and/or during and following pregnancy, and result from atrophy of the dermis and overextension of the skin; also associated with ascites and Cushing's syndrome. Synonym: atrophoderma striatum, lineae albicantes, lineae atrophicae, linear atrophy, stretch marks, stria, striae atrophicae, striate atrophy of skin, traction atrophy, vergeture. (05 Mar 2000) |
| CS2 secondary alkylsulfohydrolase | <enzyme> From comamonas terrigena Registry number: EC 3.1.6.- Synonym: cs2 sa sulfohydrolase (26 Jun 1999) |
| protein structure, secondary | The stage in the development of protein structure in which regular hydrogen-bond interactions within contiguous stretches of polypeptide chain give rise to alpha helices and beta sheets. This is the first folding level of protein building. (12 Dec 1998) |
| secondary | Second or inferior in order of time, place or importance, derived from or consequent to a primary event or thing. Origin: L. Secundarius, secundus = second (18 Nov 1997) |
| secondary abdominal pregnancy | A condition in which the embryo or foetus continues to grow in the abdominal cavity after its expulsion from the fallopian tube or other seat of its primary development. Synonym: abdominocyesis. (05 Mar 2000) |
| secondary adhesion | Delayed closure of two granulating surfaces. Synonym: secondary adhesion, secondary union. (05 Mar 2000) |
| secondary adrenocortical insufficiency | Adrenocortical insufficiency caused by failure of ACTH secretion resulting from anterior pituitary disease or inhibition of ACTH production resulting from exogenous steroid therapy. (05 Mar 2000) |
| secondary aerodontalgia | Pain referred to the dental area from an area of aerosinusitis. (05 Mar 2000) |
| secondary agammaglobulinaemia | Immunodeficiency in which there is no evident defect in the lymphoid tissues, but rather hypercatabolism or loss of immunoglobulins such as occurs in familial idiopathic hypercatabolic hypoproteinaemia or in defects associated with the nephrotic syndrome. Synonym: secondary agammaglobulinaemia, secondary antibody deficiency, secondary hypogammaglobulinaemia. (05 Mar 2000) |
| secondary alcohol | An alcohol characterised by the bivalent atom group (05 Mar 2000) |