| MTDDA | Minnesota Test for Differential Diagnosis of Aphasia |
|---|---|
| NCCEA | Neurosensory Center Comprehensive Examination for Aphasia |
| SAS | sarcoma amplified sequence; self-rating anxiety scale; short arm splint; Sklar Aphasia Scale; sleep ... |
| TCMA | transcortical motor aphasia |
| TMA | tetramethylammonium; thrombotic microangiopathy; thyroid microsomal antibody; transcortical mixed ap... |
| nonfluent aphasia | A type of aphasia in which there is a deficit in speech production or language output, often accompanied by a deficit in communicating by writing, signs, etc. The patient is aware of his impairment. Synonym: anterior aphasia, ataxic aphasia, Broca's aphasia, expressive aphasia, nonfluent aphasia. (05 Mar 2000) |
|---|---|
| syntactical aphasia | Aphasia in which the words are fairly well pronounced but are spoken in short phrases or poorly constructed sentences without articles, prepositions, or conjunctions. (05 Mar 2000) |
| impressive aphasia | Aphasia in which there is impairment in the comprehension of spoken and written words, associated with effortless, articulated, but paraphrasic, speech and writing; malformed words, substitute words, and enologisms are charcteristic. When severe, and speech is incomprehensible, it is called jargon aphasia. The patient often appears unaware of his deficit. Synonym: fluent aphasia, impressive aphasia, posterior aphasia, psychosensory aphasia, receptive aphasia, Wernicke's aphasia. (05 Mar 2000) |
| total aphasia | In which all aspects of speech and communication are severely impaired. at best, patients can understand or speak only a few words or phrases; they cannot read or write. Synonym: mixed aphasia, total aphasia. (05 Mar 2000) |
| transcortical aphasia | An aphasia in which the unaffected motor and sensory language areas are isolated from the rest of the hemispheric cortex. Subdivided into transcortical sensory and transcortical motor aphasias. (05 Mar 2000) |
| jargon aphasia | A form of aphasia characterised by an inability to construct a grammatical sentence, and the use of unintelligible or incorrect words; caused by a lesion in the dominant temporal lobe. Synonym: agrammatica, agrammatologia, jargon aphasia. (05 Mar 2000) |
| expressive aphasia | A type of aphasia in which there is a deficit in speech production or language output, often accompanied by a deficit in communicating by writing, signs, etc. The patient is aware of his impairment. Synonym: anterior aphasia, ataxic aphasia, Broca's aphasia, expressive aphasia, nonfluent aphasia. (05 Mar 2000) |
| Kussmaul's aphasia | Mutism in psychosis; a misnomer; not actually an aphasia. (05 Mar 2000) |
| fluent aphasia | Aphasia in which there is impairment in the comprehension of spoken and written words, associated with effortless, articulated, but paraphrasic, speech and writing; malformed words, substitute words, and enologisms are charcteristic. When severe, and speech is incomprehensible, it is called jargon aphasia. The patient often appears unaware of his deficit. Synonym: fluent aphasia, impressive aphasia, posterior aphasia, psychosensory aphasia, receptive aphasia, Wernicke's aphasia. (05 Mar 2000) |
| functional aphasia | Nonorganic aphasia related to conversion hysteria. (05 Mar 2000) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |
| colourectal neoplasms, hereditary nonpolyposis | A syndrome characterised by autosomal dominant inheritance, a low mean age (41 years) for occurrence of colon cancer, and a marked increase in the proportion of tumours in the proximal colon. (12 Dec 1998) |