[Hereditary thrombocytopathic thrombocytopenia. Report of 2 cases transmitted with dominant character]. 1975

C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador

Hereditary thrombocytopathic thrombocytopenia is reported in a family (mother and son) and is transmitted with dominant character of moderate to severe intensity (platelets fluctuated from less than 5,000 per mm-3 to 20,000 with sporadic higher rises), normal survivorhship, larger than normal diameter and abnormal platelet 3 factor. Comments are made on its resemblance to idiopathic thrombocytopenic purpura and stress is placed on the importance of its identification through the decision of splenectomy with negative results in these patients.

UI MeSH Term Description Entries
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D008297 Male Males
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D011697 Purpura, Thrombotic Thrombocytopenic An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases. Moschkowitz Disease,Purpura, Thrombotic Thrombopenic,Thrombotic Thrombocytopenic Purpura, Congenital,Thrombotic Thrombocytopenic Purpura, Familial,Congenital Thrombotic Thrombocytopenic Purpura,Familial Thrombotic Thrombocytopenia Purpura,Familial Thrombotic Thrombocytopenic Purpura,Microangiopathic Hemolytic Anemia, Congenital,Moschcowitz Disease,Schulman-Upshaw Syndrome,Thrombotic Microangiopathy, Familial,Thrombotic Thrombocytopenic Purpura,Upshaw Factor, Deficiency of,Upshaw-Schulman Syndrome,Familial Thrombotic Microangiopathy,Microangiopathy, Familial Thrombotic,Schulman Upshaw Syndrome,Thrombocytopenic Purpura, Thrombotic,Thrombopenic Purpura, Thrombotic,Thrombotic Thrombopenic Purpura,Upshaw Schulman Syndrome
D001772 Blood Cell Count The number of LEUKOCYTES and ERYTHROCYTES per unit volume in a sample of venous BLOOD. A complete blood count (CBC) also includes measurement of the HEMOGLOBIN; HEMATOCRIT; and ERYTHROCYTE INDICES. Blood Cell Number,Blood Count, Complete,Blood Cell Counts,Blood Cell Numbers,Blood Counts, Complete,Complete Blood Count,Complete Blood Counts,Count, Blood Cell,Count, Complete Blood,Counts, Blood Cell,Counts, Complete Blood,Number, Blood Cell,Numbers, Blood Cell
D001779 Blood Coagulation Factors Endogenous substances, usually proteins, that are involved in the blood coagulation process. Clotting Factor,Coagulation Factors,Blood Coagulation Factor,Clotting Factors,Coagulation Factor,Coagulation Factor, Blood,Coagulation Factors, Blood,Factor, Coagulation,Factors, Coagulation,Factor, Blood Coagulation,Factor, Clotting,Factors, Blood Coagulation,Factors, Clotting
D001792 Blood Platelets Non-nucleated disk-shaped cells formed in the megakaryocyte and found in the blood of all mammals. They are mainly involved in blood coagulation. Platelets,Thrombocytes,Blood Platelet,Platelet,Platelet, Blood,Platelets, Blood,Thrombocyte
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D005260 Female Females

Related Publications

C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
January 1975, Nouvelle revue francaise d'hematologie,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
January 1963, Rivista oto-neuro-oftalmologica,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
January 1973, Nouvelle revue francaise d'hematologie,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
February 2008, Journal of the Indian Medical Association,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
November 1958, The British journal of ophthalmology,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
December 1968, The American journal of pathology,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
August 1991, British journal of haematology,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
December 1972, Ceskoslovenska pediatrie,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
December 1999, Journal francais d'ophtalmologie,
C Alvarez-Amaya, and J Luis Márquez, and M Antonio Narváez, and F Gordon, and C Rodríguez, and F del Valle, and L Alvarez Amador
April 2021, Journal francais d'ophtalmologie,
Copied contents to your clipboard!