| ALS-PD | amyotrophic lateral sclerosis-parkinsonism-dementia [complex] |
|---|---|
| CPMS | chronic progressive multiple sclerosis |
| CS | calf serum; campomelic syndrome; carcinoid syndrome; cardiogenic shock; caries-susceptible; carotid ... |
| DCS | decompression sickness; dense canalicular system; diffuse cortical sclerosis; dorsal column stimulat... |
| DMS | delayed match-to-sample; delayed microembolism syndrome; demarcation membrane system; department of ... |
| inferior cerebellar peduncle | Large paired bundles of nerve fibres which develop on the dorsolateral surfaces of the upper medulla, extend under the lateral recesses of the rhomboid fossa and curve dorsally into the cerebellum medial to the middle cerebellar peduncle; composed of a larger (lateral) bundle, the restiform body, and a small (medial) bundle, the juxtarestiform body. Fibres forming this composite bundle originate from spinal neurons and medullary relay nuclei. The largest constituent (restiform body) is crossed fibres from the inferior olive; it also contains the dorsal spinocerebellar tract and cerebellar projections from the lateral reticular nucleus, the accessory cuneate nucleus, the paramedian reticular nuclei and the perihypoglossal nuclei. Vestibulocerebellar fibres are placed medially in the inferior cerebellar peduncle and are usually separately identified as the juxtarestiform body. Synonym: pedunculus cerebellaris inferior. (05 Mar 2000) |
|---|---|
| inferior surface of cerebellar hemisphere | It rests in the posterior cranial fossa and overlies the medulla; it includes the semilunaris inferior, biventer lobule, cerebellar tonsil, and flocculus. Synonym: facies inferior hemispherii cerebelli. (05 Mar 2000) |
| inferior veins of cerebellar hemisphere | Several veins draining the inferior portion of the cerebellar hemispheres; they terminate in the petrosal vein. Synonym: venae hemispherii cerebelli inferiores. (05 Mar 2000) |
| juvenile cerebellar astrocytoma | <oncology, tumour> This primary brain tumour of the cerebellum accounts for 10 to 30% of brain tumours in children. The are usually slow growing and benign. Symptoms include gait problems, clumsiness, headache and vomiting. Treatment often involves a combination of surgery, radiation therapy and chemotherapy. (27 Sep 1997) |
| layers of cerebellar cortex | The thin gray surface layer of the cerebellum, consisting of an outer molecular layer or stratum moleculare, a single layer of Purkinje cells (the ganglionic layer), and an inner granular layer or stratum granulosum. Synonym: cortex cerebelli. (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) |
| corneal dystrophies, hereditary | Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. (12 Dec 1998) |
| hereditary | <genetics> Transferred via genes from parent to child. (16 Dec 1997) |
| hereditary amyloidosis | <neurology> A disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed, an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during mid-life and is found largely in persons of Portuguese descent. Other rare clinical types occur. Inheritance: autosomal dominant. Synonym: familial amyloidosis, hereditary amyloidosis. (05 Mar 2000) |
| hereditary angioedema | 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) |
| hereditary angioneurotic oedema | 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) |