| Eponyms in category: Blood |
| 187
main and alternative
entries found.
|
|
| Abotutuo (African name) (Herrick's syndrome) |
| Sickle cell anaemia. |
| Abrami's disease (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Abrami's syndrome (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Addison's anaemia (Addison-Biermer disease) |
| Historic term for pernicious anaemia or megaloblastic anaemia, secondary to vitamin B12 deficiency. |
| Addison-Biermer anaemia (Addison-Biermer disease) |
| Historic term for pernicious anaemia or megaloblastic anaemia, secondary to vitamin B12 deficiency. |
| Addison-Biermer disease |
| Historic term for pernicious anaemia or megaloblastic anaemia, secondary to vitamin B12 deficiency. |
| Albright's anaemia |
| Anaemia seen in advanced hyperparathyroidism. |
| Alder's bodies (Alder-Reilly bodies) |
| Granular inclusions in polymorphonuclear leukocytes.
|
| Alder-Reilly bodies |
| Granular inclusions in polymorphonuclear leukocytes.
|
| Alexander's syndrome (Benjamin Alexander) |
| A congenital disorder of both sexes with onset in childhood or adult life. Like haemophilia but less severe. |
| Anémie, maladie ou syndrome de Dresbach (French) (Dresbach's anaemia) |
| A haematological disorder characterized by the presence of elliptical erythrocytes in the blood. |
| Arakawa's syndrome II |
| A congenital syndrome of tetrahydrofolate methyltransferase deficiency. |
| Arakwa-Highashi syndrome |
| Uracil-uric refractory anaemia with peroxidase negative neutrophils and megaloblastic bone marrow. |
| Arnason's syndrome |
| Amyloid cerebral deposits. |
| Ashby's techniques |
| A differential agglutination method which is used to determine survival rates of red blood cells in the human body.
|
| Astrup's micro method |
| An indirect method for measuring the acid-base status of the blood. |
| Astrup's thrombin inhibitor |
| Thermo labile coagulation factor. |
| Astrup’s microapparatus (Astrup's micro method) |
| An indirect method for measuring the acid-base status of the blood. |
| Auberger's blood group |
| Blood group with the antigen Aua. |
| Bamberger's albuminuria |
| Albuminuria occurring in later stages of severe anaemia. |
| Bandler's syndrome |
| Intestinal haemangiomatosis with mucocutaneous pigmentation. |
| Banti's disease |
| A syndrome of anaemia, congestive splenic enlargement, thrombocytopenia, leukopenia, gasterointestinal hemorrhages, portal cirrhosis, obstruction of splenic, portal, or intrahepatic veins and ultimately cirrhosis of liver. |
| Banti's syndrome (Banti's disease) |
| A syndrome of anaemia, congestive splenic enlargement, thrombocytopenia, leukopenia, gasterointestinal hemorrhages, portal cirrhosis, obstruction of splenic, portal, or intrahepatic veins and ultimately cirrhosis of liver. |
| Banti-Senator disease (Banti's disease) |
| A syndrome of anaemia, congestive splenic enlargement, thrombocytopenia, leukopenia, gasterointestinal hemorrhages, portal cirrhosis, obstruction of splenic, portal, or intrahepatic veins and ultimately cirrhosis of liver. |
| Bernard's syndrome (Jean Bernard) |
| Acute familial haemolysis. |
| Bernard-Soulier syndrome (Jean Bernard) |
| A familial and congenital bleeding disorder characterised by giant platelets and thrombocytopenia. |
| Biermer-Ehrlich anaemia (Addison-Biermer disease) |
| Historic term for pernicious anaemia or megaloblastic anaemia, secondary to vitamin B12 deficiency. |
| Cathic’s syndrome (Heinz' bodies congenital haemolytic anaemia) |
| Haemolytic anaemia of infancy associated with the finding of Heinz’ bodies in the red cells. |
| Chauffard’s syndrome (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Christmas' disease |
| A form of haemophilia caused by deficiency of Christmas’ factor. |
| Christmas' factor |
| A thromboplastin activator which is necessary for normal coagulation. |
| Chwechweechwe (African name) (Herrick's syndrome) |
| Sickle cell anaemia. |
| Cooley's anaemia |
| A lethal anaemia resulting from inheritance of a recessive trait responsible for interference with the rate of haemoglobin synthesis. |
| Cooley's anaemia II |
| Cooley's name has been attached to atype of anaemia which he described shortly before his death, but no further description have been found. |
| Cooley's anaemia syndrome (Cooley's anaemia) |
| A lethal anaemia resulting from inheritance of a recessive trait responsible for interference with the rate of haemoglobin synthesis. |
| Cooley's disease (Cooley's anaemia) |
| A lethal anaemia resulting from inheritance of a recessive trait responsible for interference with the rate of haemoglobin synthesis. |
| Cooley's syndrome (Cooley's anaemia) |
| A lethal anaemia resulting from inheritance of a recessive trait responsible for interference with the rate of haemoglobin synthesis. |
| Cooley's trait |
| Thalassaemia minor.
|
| Cooley-Lee syndrome (Cooley's anaemia) |
| A lethal anaemia resulting from inheritance of a recessive trait responsible for interference with the rate of haemoglobin synthesis. |
| Crosby's syndrome |
| A no longer commonly used term for a hereditary, non-spherocytic haemolytic anaemia caused by enzyme disorders, hemoglobinopathies, or defects in membrane structure. |
| Crosby's syndrome (misnomer) (Zuelzer-Kaplan syndrome II) |
| Haemoglobin C thalassaemia; thalassaemia-haemoglobin C disease. |
| Crosby's test |
| A diagnostic test for demonstrating the nocturnal paroxysmal heamoglobinuria. |
| Dameshek's syndrome (Cooley's anaemia) |
| A lethal anaemia resulting from inheritance of a recessive trait responsible for interference with the rate of haemoglobin synthesis. |
| Debrie’s familial haemolytic disease (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Di Guglielmo's disease |
| A syndrome of unknown origin characterised by enormous numbers of nucleated red cells appearing in the bone marrow and blood. |
| Di Guglielmo's syndrome (Di Guglielmo's disease) |
| A syndrome of unknown origin characterised by enormous numbers of nucleated red cells appearing in the bone marrow and blood. |
| Di Guglielmo’s disease II (Mortensen's syndrome) |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Di Guglielmo’s syndrome (Mortensen's syndrome) |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Dresbach's anaemia |
| A haematological disorder characterized by the presence of elliptical erythrocytes in the blood. |
| Dresbach's disease (Dresbach's anaemia) |
| A haematological disorder characterized by the presence of elliptical erythrocytes in the blood. |
| Dresbach's syndrome (Dresbach's anaemia) |
| A haematological disorder characterized by the presence of elliptical erythrocytes in the blood. |
| Dreyfus-Dausset-Widal syndrome (Lederer-Brill disease) |
| Obsolete term for an autoimmune haemolytic aneamia with extremely variable clinical features. |
| Dreyfus-Dausset-Widal syndrome (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Dyke-Young anaemia |
| An acquired form of chronic immunohaemolytic macrocytic haemolytic anaemia with increased erythrocyte fragility. |
| Dyke-Young syndrome (Lederer-Brill disease) |
| Obsolete term for an autoimmune haemolytic aneamia with extremely variable clinical features. |
| Dyke-Young syndrome (chronic macrocytic type) (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Döhle's bodies |
| Light blue-gray, basophilic, leukocute inclusions in the periphery of neutrophils (in the cytoplasm of neutrophil granulocytes), 1-3 µ in diameter. |
| Edelmann's anaemia (Edelmann's syndrome I) |
| A form of chronic infectious anaemia. |
| Edelmann's syndrome I |
| A form of chronic infectious anaemia. |
| Ehrlich hämoglobinämische Innenkörper (German) (Heinz' bodies) |
| Small irregular, deep purple granules in red blood cells due to damage of the haemoglobin molecules. |
| Ehrlich Innenkörper (German) (Heinz' bodies) |
| Small irregular, deep purple granules in red blood cells due to damage of the haemoglobin molecules. |
| Ehrlich's bodies (Heinz' bodies) |
| Small irregular, deep purple granules in red blood cells due to damage of the haemoglobin molecules. |
| Ehrlich's finger test |
| In vivo test for demonstrating a haemolysis caused by biphasic cold haemolysins (Donath-Landsteiner antibodies). |
| Epstein's syndrome (Mortensen's syndrome) |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Epstein-Goedel syndrome (Mortensen's syndrome) |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Faber's anaemia |
| A form of aneamia caused by deficient intake, absorption, or metabolism of iron. |
| Faber’s syndrome (Faber's anaemia) |
| A form of aneamia caused by deficient intake, absorption, or metabolism of iron. |
| Facteur plasmatique de Haserick (French) (Haserick's factor) |
| Thermolabile antinuclear (anti DNS) antibodies occurring in Lupus erythematodes. |
| Glanzmann's syndrome (Glanzmann's thrombastenia) |
| A rare congenital abnormality of blood platelets, characterized by easy bruising and excessive bleeding after trauma and epistaxis. |
| Glanzmann's thrombastenia |
| A rare congenital abnormality of blood platelets, characterized by easy bruising and excessive bleeding after trauma and epistaxis. |
| Glanzmann-Nägeli syndrome (Glanzmann's thrombastenia) |
| A rare congenital abnormality of blood platelets, characterized by easy bruising and excessive bleeding after trauma and epistaxis. |
| Greppi-Micheli-Rietti syndrome (Rietti-Greppi-Micheli syndrome) |
| A no longer commonly used term for heterozygous thalassaemia. |
| Gänsslen's disease |
| A familial form of constitutional leukopenia. |
| Gänsslen's syndrome (Gänsslen's disease) |
| A familial form of constitutional leukopenia. |
| Gänsslen's syndrome (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Gänsslen's syndrome II |
| Syndrome characterized by a severe degree of metabolic bone change associated with familial haemolytic anaemia. |
| Gänsslen-Erb acholuric jaundice syndrome (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Gänsslen-Erb syndrome (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Ham's test |
| The definitive test for diagnosing paroxysmal nocturnal heamoglobinuria (PNH). |
| Ham-Dacie acidified serum test (Ham's test) |
| The definitive test for diagnosing paroxysmal nocturnal heamoglobinuria (PNH). |
| Ham-Dacie test (Ham's test) |
| The definitive test for diagnosing paroxysmal nocturnal heamoglobinuria (PNH). |
| Hamburger's phenomenon |
| Erythrocyte phenomenon. |
| Haserick's factor |
| Thermolabile antinuclear (anti DNS) antibodies occurring in Lupus erythematodes. |
| Haserick's test or plasma test |
| Only French description available |
| Hayem's anaemia (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Hayem's chamber |
| Chamber for blood platelet counting.
|
| Hayem's icterus (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Hayem's solution |
| A diluting fluid for blood used in counting erythrocytes. |
| Hayem-Faber syndrome (Faber's anaemia) |
| A form of aneamia caused by deficient intake, absorption, or metabolism of iron. |
| Hayem-Sahli haemocytometer |
| A microscope used for determining the number of platelets in a stated volume of blood. |
| Hayem-Widal disease (Georges Fernand Isidore Widal) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Hayem-Widal syndrome (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Hayem-Widal-Loutit syndrome (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Hayem-Widal-Loutit syndrome (Lederer-Brill disease) |
| Obsolete term for an autoimmune haemolytic aneamia with extremely variable clinical features. |
| Hegglin’s anomaly (May-Hegglin anomaly) |
| A cytoplasmic leukocyte anomaly characterized by the presence Döhle or Amato bodies (2-5 µ) in neutrophils and eosinophils, thrombocytopenia, and giant blood platelets. |
| Hegglin’s syndrome (May-Hegglin anomaly) |
| A cytoplasmic leukocyte anomaly characterized by the presence Döhle or Amato bodies (2-5 µ) in neutrophils and eosinophils, thrombocytopenia, and giant blood platelets. |
| Heinz bodies-congenital haemolytic anaemia syndrome (Heinz' bodies congenital haemolytic anaemia) |
| Haemolytic anaemia of infancy associated with the finding of Heinz’ bodies in the red cells. |
| Heinz' bodies |
| Small irregular, deep purple granules in red blood cells due to damage of the haemoglobin molecules. |
| Heinz' bodies congenital haemolytic anaemia |
| Haemolytic anaemia of infancy associated with the finding of Heinz’ bodies in the red cells. |
| Heinz' body anaemia (Heinz' bodies congenital haemolytic anaemia) |
| Haemolytic anaemia of infancy associated with the finding of Heinz’ bodies in the red cells. |
| Heinz-Ehrlich bodies (Heinz' bodies) |
| Small irregular, deep purple granules in red blood cells due to damage of the haemoglobin molecules. |
| Hermansky's syndrome (Hermansky-Pudlak syndrome) |
| A hereditary platelet defect resulting in a bleeding tendency, albinism and lung disease. |
| Hermansky-Pudlak syndrome |
| A hereditary platelet defect resulting in a bleeding tendency, albinism and lung disease. |
| Herrick's syndrome |
| Sickle cell anaemia. |
| Howell-Gram method |
| Method of determining the coagulation time of blood: citrate plasma in small vitrios is kept at 37º C in transparent Dewar vessel. |
| Hunter-Addison anaemia (Addison-Biermer disease) |
| Historic term for pernicious anaemia or megaloblastic anaemia, secondary to vitamin B12 deficiency. |
| Hutinel-Tixier syndrome (Tixier's syndrome) |
| An obsolete term for a fulminating haemolytic crisis in debilitated or malnourished newborns. |
| Kaznelson’s syndrome (Faber's anaemia) |
| A form of aneamia caused by deficient intake, absorption, or metabolism of iron. |
| Kelly's syndrome (Plummer-Vinson syndrome) |
| A syndrome characterized by an iron-deficiency anaemia, atrophic changes in the buccal, glossopharyngeal, and oesophageal mucous membranes, koilonycha (spoon-shaped finger nails), and dysphagia. |
| Knud Faber’s syndrome (Faber's anaemia) |
| A form of aneamia caused by deficient intake, absorption, or metabolism of iron. |
| Korovnikov's disease (Korovnikov's syndrome) |
| A special form of Banti's disease characterised by splenomegaly with subthrombocytosis and gastrointestinal haemorrhage. |
| Korovnikov's syndrome |
| A special form of Banti's disease characterised by splenomegaly with subthrombocytosis and gastrointestinal haemorrhage. |
| Lebert's essential anaemia (Addison-Biermer disease) |
| Historic term for pernicious anaemia or megaloblastic anaemia, secondary to vitamin B12 deficiency. |
| Lederer acute anaemia (Lederer's anaemia) |
| An acute, transient type of Lederer-Brill disease. A form of acute haemolytic anaemia of infectious origin, with rapid onset and recovery in children.
|
| Lederer's anaemia |
| An acute, transient type of Lederer-Brill disease. A form of acute haemolytic anaemia of infectious origin, with rapid onset and recovery in children.
|
| Lederer-Brill disease |
| Obsolete term for an autoimmune haemolytic aneamia with extremely variable clinical features. |
| Lederer-Brill syndrome (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Lederer’s anaemia (acute transient type) (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Lederer’s disease (Lederer-Brill disease) |
| Obsolete term for an autoimmune haemolytic aneamia with extremely variable clinical features. |
| Lee and White method |
|
| Levine-Critchley syndrome |
| Acanthocytosis with neurologic disease, choreoacanthocytosis, neuroacanthocytosis.
|
| Loutit's syndrome |
| Jaundice and haemolytic anaemia associated with hyperbilirubunaemia. |
| Löffler's endocarditis |
| A very rare form of endocarditis associated with a highly increased number of eosinophilic granulocytes in the blood. |
| Löffler's endomyocarditis (Löffler's endocarditis) |
| A very rare form of endocarditis associated with a highly increased number of eosinophilic granulocytes in the blood. |
| Löffler’s fibroblastic endocarditis (Löffler's endocarditis) |
| A very rare form of endocarditis associated with a highly increased number of eosinophilic granulocytes in the blood. |
| Løffler’s syndrome (Löffler's endocarditis) |
| A very rare form of endocarditis associated with a highly increased number of eosinophilic granulocytes in the blood. |
| May-Hegglin anomaly |
| A cytoplasmic leukocyte anomaly characterized by the presence Döhle or Amato bodies (2-5 µ) in neutrophils and eosinophils, thrombocytopenia, and giant blood platelets. |
| May-Hegglin syndrome (May-Hegglin anomaly) |
| A cytoplasmic leukocyte anomaly characterized by the presence Döhle or Amato bodies (2-5 µ) in neutrophils and eosinophils, thrombocytopenia, and giant blood platelets. |
| Micheli-Rietti syndrome (Rietti-Greppi-Micheli syndrome) |
| A no longer commonly used term for heterozygous thalassaemia. |
| Minkowski-Chauffard disease |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Minkowski-Chauffard haemolytic jaundice (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Minkowski-Chauffard-Gänsslen syndrome (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Morbus Minkowski-Chauffard (Minkowski-Chauffard disease) |
| Congenital haemolytical anaemia presenting with spherocytosis, splenomegaly and varying degrees of anaemia and ikterus. |
| Mortensen's syndrome |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Mortensen’s disease (Mortensen's syndrome) |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Neumann's cells (Franz Ernst Christian Neumann) |
| Nucleated, stained cells in the bone marrow in which red blood corpuscles originate. |
| nuiduidui (Herrick's syndrome) |
| Sickle cell anaemia. |
| Nuiduidui (African name) (Herrick's syndrome) |
| Sickle cell anaemia. |
| Nwiiwii (African name) (Herrick's syndrome) |
| Sickle cell anaemia. |
| Nygaard-Brown syndrome (George Elgie Brown) |
| A syndrome of arterial occlusion with reduced bleeding and coagulation time. |
| Nägeli syndrome II (Glanzmann's thrombastenia) |
| A rare congenital abnormality of blood platelets, characterized by easy bruising and excessive bleeding after trauma and epistaxis. |
| Osler's disease (Vaquez' disease) |
| A relatively rare chronic disease of the blood in which the red cells are increased in number. The spleen becomes enlarged, and the face is a deep red rather than truly cyanotic. |
| Osler-Vaquez disease (Vaquez' disease) |
| A relatively rare chronic disease of the blood in which the red cells are increased in number. The spleen becomes enlarged, and the face is a deep red rather than truly cyanotic. |
| Pagon's syndrome |
| Congenital anaemia with ataxia, clonus, and positive Babinski sign. |
| Paterson-Brown-Kelly syndrome (Plummer-Vinson syndrome) |
| A syndrome characterized by an iron-deficiency anaemia, atrophic changes in the buccal, glossopharyngeal, and oesophageal mucous membranes, koilonycha (spoon-shaped finger nails), and dysphagia. |
| Paterson-Kelly syndrome (Plummer-Vinson syndrome) |
| A syndrome characterized by an iron-deficiency anaemia, atrophic changes in the buccal, glossopharyngeal, and oesophageal mucous membranes, koilonycha (spoon-shaped finger nails), and dysphagia. |
| Paterson’s syndrome (Plummer-Vinson syndrome) |
| A syndrome characterized by an iron-deficiency anaemia, atrophic changes in the buccal, glossopharyngeal, and oesophageal mucous membranes, koilonycha (spoon-shaped finger nails), and dysphagia. |
| Plummer-Vinson syndrome |
| A syndrome characterized by an iron-deficiency anaemia, atrophic changes in the buccal, glossopharyngeal, and oesophageal mucous membranes, koilonycha (spoon-shaped finger nails), and dysphagia. |
| Rabe-Salomon syndrome |
| A familial blood-clotting disorder that manifests from birth with bleeding from umbilical cord. |
| Révol's syndrome (Glanzmann's thrombastenia) |
| A rare congenital abnormality of blood platelets, characterized by easy bruising and excessive bleeding after trauma and epistaxis. |
| Revol’s disease (Mortensen's syndrome) |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Revol’s syndrome (Mortensen's syndrome) |
| Obsolete, no longer used term for essential thrombocythaemia, a haematological disorder characterized by prolonged bleeding time and splenomegaly, with excessive bleeding after minor trauma and at surgery. |
| Rietti's disease (Rietti-Greppi-Micheli syndrome) |
| A no longer commonly used term for heterozygous thalassaemia. |
| Rietti-Greppi-Micheli syndrome |
| A no longer commonly used term for heterozygous thalassaemia. |
| Rietti-Greppi-Micheli syndrome II |
| This term has been used to designate a group of the hereditary haemopathic syndromes. |
| Rundles-Falls syndrome |
| A hereditary form of familial sideroblastic anaemia, occurring in males. |
| Sahli's apparatus |
| Instrument used in Sahli's method for determination of haemoglobin. |
| Sahli's method I |
| One of the original techniques for measuring haemoglobin calorimetrically, with a haemometer. |
| Sahli’s tube (Sahli's apparatus) |
| Instrument used in Sahli's method for determination of haemoglobin. |
| Salomon’s syndrome (Eugen Salomon) (Rabe-Salomon syndrome) |
| A familial blood-clotting disorder that manifests from birth with bleeding from umbilical cord. |
| Schilling's classification and haemogram |
| A differential count of the leukocytes, in which the polymorphonuclear neutrophil cells are divided into four categories according to number and arrangement of the nuclei in the cells. |
| Schilling's type of leukaemia |
| Monocytic leukaemia without any morphological components resembling a myelocytic origin. |
| Schilling’s leukaemia (Schilling's type of leukaemia) |
| Monocytic leukaemia without any morphological components resembling a myelocytic origin. |
| Senator syndrome (Banti's disease) |
| A syndrome of anaemia, congestive splenic enlargement, thrombocytopenia, leukopenia, gasterointestinal hemorrhages, portal cirrhosis, obstruction of splenic, portal, or intrahepatic veins and ultimately cirrhosis of liver. |
| Silvestroni-Bianco anaemia |
| No longer used term for heterozygotous thalassaemia. |
| Silvestroni-Bianco syndrome (Silvestroni-Bianco anaemia) |
| No longer used term for heterozygotous thalassaemia. |
| Soulier-Boffa syndrome |
| Repeated spontaneous abortions in women with circulatory antithromboplastin anticoagulant and thrombosis. |
| Tixier's syndrome |
| An obsolete term for a fulminating haemolytic crisis in debilitated or malnourished newborns. |
| Trousseau's syndrome (Nygaard-Brown syndrome (George Elgie Brown)) |
| A syndrome of arterial occlusion with reduced bleeding and coagulation time. |
| Vaques-Osler arythremia (Vaquez' disease) |
| A relatively rare chronic disease of the blood in which the red cells are increased in number. The spleen becomes enlarged, and the face is a deep red rather than truly cyanotic. |
| Vaquez' disease |
| A relatively rare chronic disease of the blood in which the red cells are increased in number. The spleen becomes enlarged, and the face is a deep red rather than truly cyanotic. |
| Vaquez' polycythaemia (Vaquez' disease) |
| A relatively rare chronic disease of the blood in which the red cells are increased in number. The spleen becomes enlarged, and the face is a deep red rather than truly cyanotic. |
| Vaquez-Osler disease (Vaquez' disease) |
| A relatively rare chronic disease of the blood in which the red cells are increased in number. The spleen becomes enlarged, and the face is a deep red rather than truly cyanotic. |
| Waldenström-Kjellberg syndrome (Plummer-Vinson syndrome) |
| A syndrome characterized by an iron-deficiency anaemia, atrophic changes in the buccal, glossopharyngeal, and oesophageal mucous membranes, koilonycha (spoon-shaped finger nails), and dysphagia. |
| Widal Probe (German). (Widal's haemoclastic crisis (Georges Fernand Isidore Widal)) |
| A leukocyte phenomenon. |
| Widal's disease (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Widal's haemoclastic crisis (Georges Fernand Isidore Widal) |
| A leukocyte phenomenon. |
| Widal, Abrami and Brulé haemolytic icterus (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Widal-Ravaut disease (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Widal’s syndrome (Hayem-Widal disease (Georges Fernand Isidore Widal)) |
| A now obsolete term for a haematological disorder clinically characterised by decreased red blood count, spherocytosis, icterus, and splenomegaly. |
| Witebsky-substances |
| Substances specific for ABO blood-groups extracted from horse and pig stomachs. |
| Witts’ anaemia (Faber's anaemia) |
| A form of aneamia caused by deficient intake, absorption, or metabolism of iron. |
| Witts’ syndrome (Faber's anaemia) |
| A form of aneamia caused by deficient intake, absorption, or metabolism of iron. |
| Zuelzer's syndrome |
| An association of eosinophilia, leukocytosis, and hypergammaglobulinemia. |
| Zuelzer-Kaplan syndrome I (Crosby's syndrome) |
| A no longer commonly used term for a hereditary, non-spherocytic haemolytic anaemia caused by enzyme disorders, hemoglobinopathies, or defects in membrane structure. |
| Zuelzer-Kaplan syndrome II |
| Haemoglobin C thalassaemia; thalassaemia-haemoglobin C disease. |
| Zuelzer-Ogden syndrome |
| A megaloblastic anaemia with a superimposed infection and deficiency of vitamin C, observed in children. |
|
