| DPT | Demerol, Phenergan, and Thorazine; dermatopontin; dichotic pitch discrimination test; diphtheria-per... |
|---|---|
| ACA | abnormal coronary artery; acrodermatitis chronica atrophicans; acute cerebellar ataxia; adenocarcino... |
| ADR | activation, depression, repetition [in bone remodeling]; adrenodoxin reductase; Adriamycin; adverse ... |
| AEM | Academic Emergency Medicine [journal]; analytical electron microscopy; ambulatory electrocardiograph... |
| AEMK | ataxia episodica with myokymia |
| AT | Ataxia Telangiectasis |
|---|---|
| ATM | Ataxia Telangiectasia Mutated |
| ADCA | Autosomal Dominant Cerebellar Ataxia |
| FA | Friedreich ataxia |
| FRDA | Friedreich ataxia |
| diphtheritic | <medicine> 1. Pertaining to, or connected with, diphtheria. 2. Having characteristics resembling those of diphtheria; as, diphtheritic inflammation of the bladder. Source: Websters Dictionary (01 Mar 1998) |
|---|---|
| diphtheritic conjunctivitis | A severe conjunctival inflammation caused by Corynebacterium diphtheriae and characterised by an infiltrating membrane which on removal leaves a raw surface. Synonym: membranous conjunctivitis. (05 Mar 2000) |
| diphtheritic enteritis | Enteritis with the formation of a membrane or a false membrane. See: pseudomembranous enterocolitis. (05 Mar 2000) |
| diphtheritic membrane | The false membrane forming on the mucous surfaces in diphtheria. (05 Mar 2000) |
| diphtheritic neuropathy | A rapidly developing peripheral neuropathy caused by a toxin elaborated by Corynebacterium diphtheriae. (05 Mar 2000) |
| diphtheritic paralysis | <otolaryngology> Paralysis affecting the uvula most frequently, but also any other muscle, due to toxic neuritis; usually appears in the second or third week following the beginning of the attack of diphtheria. Synonym: diphtheritic paralysis. (05 Mar 2000) |
| diphtheritic ulcer | An ulcer covered with a gray adherent membrane, caused by Corynebacterium diphtheriae. (05 Mar 2000) |
| acute ataxia | Generalised ataxia of abrupt onset, most often caused by drug intoxications, poisonings, or vestibular neuronitis. (05 Mar 2000) |
| ataxia | <neurology> Failure of muscular coordination, irregularity of muscular action. Origin: Gr. Taxis = order (16 Dec 1997) |
| ataxia cordis | <cardiology> A condition where there is disorganised electrical conduction in the atria, resulting in ineffective pumping of blood into the ventricle. Acronym: AF (02 Jan 1998) |
| ataxia of calves | A specific cerebellar ataxia in the Jersey breed, probably a recessive genetic trait. (05 Mar 2000) |
| ataxia of lambs | Myelination failure seen in ewes on a copper-deficient diet. (05 Mar 2000) |
| ataxia-telangiectasia | <neurology, oncology> An intriguing autosomal recessive disorder in which a single defective gene produces myriad and protean effects, presents with cerebellar ataxia, telangiectasias in the eyes and skin, immune deficiency and autoimmune phenomena, propensity for lymphoid and other malignancies, excessive sensitivity to ionising radiation, increased serum alpha-fetoprotein concentrations and a tendency for chromosome breakage and translocation. A syndrome characterised by choreoathetosis beginning in childhood, progressive cerebellar ataxia, telangiectasis of conjunctiva and skin, slowly progressive mental deterioration and increasing cerebellar degeneration. There is evidence that heterozygotes show an increased susceptibility to malignancy as well, with breast cancer often cited. The gene was localised by linkage studies to chromosome 11q22-23, and recently cloned, revealing it to be homologous to the PI-3 kinase family so that prenatal diagnosis by RFLP analysis is possible. Other related genes are suspected to exist. Diagnosis in affected patients is made on clinical grounds, by detection of high concentrations of alpha-fetoprotein, and by a specialised cell culture assay for radiosensitivity and atypical radioresistant DNA synthesis. These cell culture methods are also used for prenatal diagnosis. A characteristic autopsy feature of ataxia-telangiectasia is the presence of empty basket cells in the cerebellum which results from degeneration of the previously contained Purkinje cells. Inheritance: autosomal recessive. (16 Dec 1998) |
| ataxia telangiectasia syndrome | ataxia telangiectasia |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
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