| Eponyms in category: Various |
| 69
main and alternative
entries found.
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| Ackerman's tumour |
| A rare locally malignant tumor which is malignant in behaviour but whose pathology is relatively benign. |
| Ackermann’s carcinoma (Ackerman's tumour) |
| A rare locally malignant tumor which is malignant in behaviour but whose pathology is relatively benign. |
| Aeby's plane |
| A craniometric plane. It passes through the nasion and basion perpendicular to the median plane. |
| Albarran's law |
| "Le rein malade a un débit beaucoup plus constant que le rein sain et son fonctionnement varie d'autant moins d'un moment à l'autre que son parenchyme est plus détruit."
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| Albright hereditary osteodystrophy (Albright's syndrome II) |
| This title has been used to exemplify the effects of failure of an end organ to respond in a normal way to is corresponding hormone. Deficiency of hormone is not a factor. |
| Albright's syndrome II |
| This title has been used to exemplify the effects of failure of an end organ to respond in a normal way to is corresponding hormone. Deficiency of hormone is not a factor. |
| Alexander's technique (Frederick Matthias Alexander) |
| An educational process that teaches students how to properly coordinate body and mind to release harmful tension and to improve posture, coordination and general health. |
| Alvarez' syndrome |
| A syndrome of hysterical or neurotic abdominal bloating without any excess of gas in the digestive tract. |
| Arloing's phenomenon |
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| Arneth's count |
| Classification of poly-morphonuclear neutrophils or eosinophile leukocytes in groups or class with the help of differential counting based on the number of lobes (1 - 5) in the nucleus. |
| Arneth's syndrome |
| A condition characterized by auscultory sound modifications - muffling of the palpable thrill during speech – caused by complete hepatisation of lung tissue. |
| Arneth’s classification of neutrophils (Arneth's count) |
| Classification of poly-morphonuclear neutrophils or eosinophile leukocytes in groups or class with the help of differential counting based on the number of lobes (1 - 5) in the nucleus. |
| Arnold's canal |
| A passage of the petrous portion of the temporal bone for the auricular branch of the vagus. |
| Arnold's reaction (Arnold's test) |
| Test for demonstrating nephrorosein, a pathological urine pigment that can be distinguished from urorosein by spectrographical methods. |
| Arnold's test |
| Test for demonstrating nephrorosein, a pathological urine pigment that can be distinguished from urorosein by spectrographical methods. |
| Asherson's syndrome |
| Achalasia of the cricopharyngeal sphincter, with dysphagia followed immediately by episodes of coughing.
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| Asperger's syndrome |
| A serious disorder resembling autism. |
| Asperger’s disorder (Asperger's syndrome) |
| A serious disorder resembling autism. |
| Babcock's test |
| Test to determine the amount of butterfat in milk by centrifuging a mixture of equal parts of milk and sulphuric acid. |
| Babcock's test for milk (Babcock's test) |
| Test to determine the amount of butterfat in milk by centrifuging a mixture of equal parts of milk and sulphuric acid. |
| Babès Knötchen (German) (Babès-Ernst granules) |
| Protoplasmic inclusions occurring in the protoplasm of various gram-positive bacteria, in algae, swamps and protozoa. |
| Babès-Ernst granules |
| Protoplasmic inclusions occurring in the protoplasm of various gram-positive bacteria, in algae, swamps and protozoa. |
| Baer's vesicle |
| The vesicular ovarian follicle. |
| Baker's disease |
| Defect of the periarticular ligaments.
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| Bamberger's disease II |
| Progressive polyserositis with effusion of fluid into the pleural and peritoneal cavities. |
| Bamberger-Concato disease (Bamberger's disease II) |
| Progressive polyserositis with effusion of fluid into the pleural and peritoneal cavities. |
| Bar's syndrome |
| Eponym used ot indicare manifestations of abdominal pains and presence of bacteria in the urine during pregnancy.
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| Bebesia |
| Piroplasma; a genus of the order Haemosporidia that consists of parasites - intra-cellular non-pigmented sporozoa - found in the blood of cattle, sheep, horses, dogs, and other vertebrate animals. |
| Biber-Haab-Dimmer degeneration |
| A localised form of amyloidosis manifested by progressive corneal opacity with distinct borders and a network of lattice-like branching filaments. |
| Brocq's syndrome I (Vidal's syndrome) |
| A skin disease marked by the appearance of localized and circumscribed patches of thickened skin with lichenification, becoming scaly, resulting from repetitive rubbing and scratching subsequent to pruritogenic stimuli. |
| Brodie-Trendelenburg percussion test |
| Test for incompetent valves in superficial veins. |
| Bücklers' syndrome II (Biber-Haab-Dimmer degeneration) |
| A localised form of amyloidosis manifested by progressive corneal opacity with distinct borders and a network of lattice-like branching filaments. |
| Chauffard-Ramon syndrome (Still's disease or syndrome) |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Chauffard-Ramon-Still disease (Still's disease or syndrome) |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Chauffard-Still syndrome (Still's disease or syndrome) |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Codman's sign |
| A sign seen in the absence of rotator cuff function or when there is a rupture of the supraspinatus tendon. |
| Concato's disease |
| Tuberculous inflammation of the serous membrane. |
| Dimmer's keratitis |
| A highly infectious form of keratitis marked by numerous coin-shaped or round, discrete greyish areas scattered throughout the various layers of the cornea. |
| Dreier's syndrome (Still's disease or syndrome) |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Ehrmann's syndrome |
| Arteriopathy with flash-shaped or grid-shaped dark livid skin changes of symptomatic or idiopathic aetiology. |
| Forbes-Albright syndrome |
| A syndrome characterised by galactorrhea and amenorrhoa sequenz. |
| Griesinger-Kussmaul sign (Kussmaul's pulse or sign) |
| A manifestation of limited expansion of the right ventricle. |
| Haab's degeneration (Biber-Haab-Dimmer degeneration) |
| A localised form of amyloidosis manifested by progressive corneal opacity with distinct borders and a network of lattice-like branching filaments. |
| Haab-Dimmer syndrome (Biber-Haab-Dimmer degeneration) |
| A localised form of amyloidosis manifested by progressive corneal opacity with distinct borders and a network of lattice-like branching filaments. |
| Haab’s syndrome (Biber-Haab-Dimmer degeneration) |
| A localised form of amyloidosis manifested by progressive corneal opacity with distinct borders and a network of lattice-like branching filaments. |
| Hutchinson's dehidrosis |
| A condition described by Hutchinson. See his own text. |
| Kanner's syndrome (Asperger's syndrome) |
| A serious disorder resembling autism. |
| Kussmaul's pulse or sign |
| A manifestation of limited expansion of the right ventricle. |
| Loi d'Albarran. (Albarran's law) |
| "Le rein malade a un débit beaucoup plus constant que le rein sain et son fonctionnement varie d'autant moins d'un moment à l'autre que son parenchyme est plus détruit."
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| Michaelis-Gutmann body |
| Basophilic inclusions in the cytoplasm containing calcium and iron seen in malacoplakia. |
| Paget's disease of bone |
| Medium common skeletal disease with chronic inflammation of bones, resulting in thickening and softening of bones, and bowing of long bones. |
| Paget’s disease (Paget's disease of bone) |
| Medium common skeletal disease with chronic inflammation of bones, resulting in thickening and softening of bones, and bowing of long bones. |
| Pozzi's senile pseudorickets (misnomer) (Paget's disease of bone) |
| Medium common skeletal disease with chronic inflammation of bones, resulting in thickening and softening of bones, and bowing of long bones. |
| Reis-Bücklers syndrome (Biber-Haab-Dimmer degeneration) |
| A localised form of amyloidosis manifested by progressive corneal opacity with distinct borders and a network of lattice-like branching filaments. |
| Schanz' syndrome II |
| A syndrome comprising the combined features of the lateral sclerosis and the anterior cornual syndromes. |
| Senator's angina |
| An acute and rapidly fatal form of pharyngolaryngeal infection described by Senator in 1888.
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| Snellen's sutures |
| Operation for entropion musculare. |
| Still's arthritis (Still's disease or syndrome) |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Still's disease (Still's disease or syndrome) |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Still's disease or syndrome |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Still-Chauffard-Felty syndrome (Still's disease or syndrome) |
| A rare chronic, inflammatory, systemic disease which may cause joint or connective tissue damage and visceral lesions throughout the body. |
| Stiller's sign |
| Floating tenth rib. |
| Stillers Kostalstigma (German) (Stiller's sign) |
| Floating tenth rib. |
| Stiller’s rib (Stiller's sign) |
| Floating tenth rib. |
| Vidal's syndrome |
| A skin disease marked by the appearance of localized and circumscribed patches of thickened skin with lichenification, becoming scaly, resulting from repetitive rubbing and scratching subsequent to pruritogenic stimuli. |
| Vidal's type |
| A type of deforming rheumatism affecting the fingers. |
| Vidal’s disease (Vidal's syndrome) |
| A skin disease marked by the appearance of localized and circumscribed patches of thickened skin with lichenification, becoming scaly, resulting from repetitive rubbing and scratching subsequent to pruritogenic stimuli. |
| Welcker's angle |
| The anterior inferior angle of the parietal bone. |
| Willis' glands |
| Corpora albicantia. Obsolete term. |
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