ABSTRACT
Detailed studies on the rare disorder X-linked thrombocytopenia showed that it resembles the Wiskott-Aldrich syndrome (WAS) in inheritance, clinical bleeding tendency, platelet morphology, marked thrombocytopenia and microplatelets. The calculated platelet mass was 5% of normal. Functional and biochemical studies indicated qualitatively normal aggregation and release mechanisms, whereas a moderate storage pool defect was present. The classical platelet membrane glycoproteins and lymphocyte sialophorin (CD 43) were normal. The reason for the bleeding tendency was concluded to be deficient hemostatic plug formation resulting from the low platelet mass and a moderate storage pool defect. The only clear distinction from WAS was the normal immunofunctional tests, the moderate tendency to infections and the absence of eczema. We therefore consider the trait as an attenuated form of WAS. That women are affected may indicate a particular variant.
Subject(s)
Blood Platelet Disorders/blood , Genetic Linkage , Thrombocytopenia/blood , Wiskott-Aldrich Syndrome/blood , X Chromosome , Adenosine Diphosphate/blood , Adenosine Triphosphate/blood , Adolescent , Bleeding Time , Blood Coagulation/physiology , Blood Platelets/pathology , Blood Platelets/physiology , Humans , Lymphocytes/pathology , Lymphocytes/physiology , Male , Pedigree , Platelet Count , Platelet Membrane Glycoproteins/metabolism , Severity of Illness Index , Thrombocytopenia/genetics , Wiskott-Aldrich Syndrome/geneticsABSTRACT
Polymorphism of a platelet protein is described. The gene products are represented by two peptides of MW around 30 kD. The allele frequency was estimated to 0.85 and 0.15, the common variant being of slightly higher MW and about 2 charge units more acidic than the other. The peptides were neither released nor phosphorylated, and subcelluar fractionation indicated localization to the cytosol. Attempts to raise antibodies failed, and further characterization could not be done, but the peptides seem to differ from all reasonably well characterized platelet proteins so far.
Subject(s)
Blood Platelets/chemistry , Peptides/blood , Polymorphism, Genetic , Alleles , Cytosol/chemistry , Gene Frequency , Humans , Isoelectric Point , Molecular Weight , Peptides/chemistry , Peptides/geneticsABSTRACT
Six families with total kininogen deficiency have been described in the literature. We report herein an additional case in a Pakistanese woman. The defect was discovered accidentally due to lack of normal clot formation in a preoperative routine blood sample. She had a borderline prolonged bleeding time, and reported occasional hematuria, but was otherwise without symptoms. Absence of both kininogen species was proven by functional and immunological methods, and by lack of kinin formation both by plasma kallikrein and hog pancreas kallikrein. Prekallikrein was reduced, probably because the main part circulates complexed to high molecular kininogen. Activation of intrinsic fibrinolysis was grossly hampered, and cold activation of coagulation absent with epsilonaminocaproic acid and greatly retarded by dextran sulfate, kaolin and ellagic acid. Together with other evidence the findings indicate the following order of importance for contact activation in plasma--F.XII, high molecular weight kininogen, prekallikrein.