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Werdnig, Guido <person> Austrian neurologist, 1862-1919.
See: Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
werdnig-hoffmann disease A recessively inherited acute infantile form of motor neuropathy with proximal muscle wasting particularly of the upper extremities. The chronic childhood form may be an arrested werdnig-hoffmann disorder.
(12 Dec 1998)
Werdnig-Hoffmann 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)
Werlhof's disease An obsolete term for idiopathic thrombocytopenic purpura.
(05 Mar 2000)
Werlhof, Paul <person> German physician, 1699-1767.
See: Werlhof's disease.
(05 Mar 2000)
Wermer's syndrome <syndrome> This is a hereditary disorder in which two or more of the following glands: parathyroid, pancreas, pituitary, adrenals or thyroid develop hyperplasia or a tumour.
(27 Sep 1997)
Wernekinck's commissure The decussation of the brachia conjunctiva before their entrance into the red nucleus of the tegmentum.
(05 Mar 2000)
Wernekinck's decussation The decussation of the left and right superior cerebellar peduncles in the tegmentum of the caudal mesencephalon.
Synonym: decussatio pedunculorum cerebellarium superiorum, decussatio brachii conjunctivi, decussation of brachia conjunctiva, Wernekinck's decussation.
(05 Mar 2000)
Wernekinck, Friedrich <person> German anatomist and physician, 1798-1835.
See: Wernekinck's commissure, Wernekinck's decussation.
(05 Mar 2000)
werner syndrome <radiology> Cataract in connection with scleroderma, rare; unknown aetiology, M = F, premature aging, short stature, thin, atrophic extremities, generalised osteoporosis, accelerated atherosclerosis (calcification of arteries, heart valves), beaked nose, multiple infections (including osteomyelitis), scleroderma-like skin changes, increased incidence of malignancy: GI tract, lung, kidney, ovary, breast
(12 Dec 1998)
Werner's syndrome <syndrome> A disorder consisting of scleroderma-like skin changes, bilateral juvenile cataracts, progeria, hypogonadism, and diabetes mellitus; autosomal recessive inheritance.
(05 Mar 2000)
Werner's test A thyroid function test used to diagnose difficult cases of hyperthyroidism, now largely replaced by the thyrotropin-releasing hormone stimulation test; triiodothyronine is administered for a week to 10 days, and a reduction of its uptake by the thyroid gland to less than half of the initial uptake is a normal response.
Synonym: Werner's test.
(05 Mar 2000)
Werner, F <person> Early 20th century German chemist.
See: Werner's test.
(05 Mar 2000)
Werner, Otto <person> German physician, *1879.
See: Werner's syndrome.
(05 Mar 2000)
werner-his disease Named for the German physician heinrich werner (not the werner of werner's syndrome) and the swiss physician wilhelm his, jr. (who described the bundle of his in the heart). See fever, wolhynia.
(12 Dec 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 2 ÆäÀÌÁö: 1
  • Werner Syndrome - »õâ An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease.
    Synonyms : Werner's Syndrome, Adult Progeria, Syndrome, Werner, Syndrome, Werner's, Werners Syndrome
  • Wernicke Encephalopathy - »õâ An acute neurological disorder characterized by the triad of ophthalmoplegia, ataxia, and disturbances of mental activity or consciousness. Eye movement abnormalities include nystagmus, external rectus palsies, and reduced conjugate gaze. THIAMINE DEFICIENCY and chronic ALCOHOLISM are associated conditions. Pathologic features include periventricular petechial hemorrhages and neuropil breakdown in the diencephalon and brainstem. Chronic thiamine deficiency may lead to KORSAKOFF SYNDROME. (Adams et al., Principles of Neurology, 6th ed, pp1139-42; Davis & Robertson, Textbook of Neuropathology, 2nd ed, pp452-3)
    Synonyms : Encephalopathy, Gayet-Wernicke, Encephalopathy, Wernicke's, Gayet-Wernicke Encephalopathy, Wernicke Disease, Wernicke Polioencephalitis, Superior Hemorrhagic, Wernicke Superior Hemorrhagic Polioencephalitis, Wernicke Syndrome, Wernicke's Disease
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Werlhof's disease thrombocytopenic purpura: purpura associated with a reduction in circulating blood platelets which can result from a variety of factors
Ãâó: wordnet.princeton.edu/perl/webwn
Wernicke's aphasia aphasia characterized by fluent but meaningless speech and severe impairment of the ability understand spoken or written words
Ãâó: wordnet.princeton.edu/perl/webwn
Wernicke's center Wernicke's area: the auditory word center; located in the posterior part of the superior temporal convolution in most people
Ãâó: wordnet.princeton.edu/perl/webwn
Wernicke's encephalopathy inflammatory degenerative disease of the brain caused by thiamine deficiency that is usually associated with alcoholism
Ãâó: wordnet.princeton.edu/perl/webwn
Wernicke's encephalopathy a neurological disorder characterized by confusion, apathy, drowsiness, ataxia of gait, nystagmus, and ophthalmoplegia. It was first described by Wernicke in 1881 and is now known to be due to thiamine deficiency, usually from chronic alcohol abuse. It is almost invariably accompanied by or followed by Korsakoff's syndrome (organic amnesia) and frequently accompanied by other nutritional polyneuropathies. Called also Wernicke's disease or syndrome. ...
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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WER autosomal recessive disease in which the degeneration of spinal nerve cells and brain nerve cells leads to atrophy of skeletal muscles and flaccid paralysis
WER a monster able to change appearance from human to wolf
WER United States writer (1890-1945)
WER purpura associated with a reduction in circulating blood platelets which can result from a variety of factors
WER German mathematical physicist noted for stating the uncertainty principle (1901-1976)
WER United States rocket engineer (born in Germany where he designed a missile used against England)
WER United States rocket engineer (born in Germany where he designed a missile used against England)
WER German neurologist best known for his studies of aphasia (1848-1905)
WER aphasia characterized by fluent but meaningless speech and severe impairment of the ability understand spoken or written words
WER the auditory word center
WER the auditory word center
WER inflammatory degenerative disease of the brain caused by thiamine deficiency that is usually associated with alcoholism
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