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485 Possible Causes for Deficiency, Stuart Prower

Did you mean: Deficiency, Stuart, Prower

  • Factor X Deficiency

    Liver disease and coumarin anticoagulant administration can cause factor X deficiency, together with deficiencies in other coagulation factors.[symptoma.com] Abstract Stuart Prower factor (Factor X) deficiency is a rare hereditary autosomal recessive coagulation disorder.[ncbi.nlm.nih.gov] Abstract Factor X deficiency (also known as Stuart-Prower factor deficiency) is an extremely rare hereditary hematologic disorder, affecting 1 person in 2 million.[ncbi.nlm.nih.gov]

  • Factor V Deficiency

    (congenital factor X deficiency) (see also Defect, coagulation) 286.3 Stuart-Prower (congenital factor X deficiency) (see also Defect, coagulation) 286.3 Dysfibrinogenemia[icd9data.com] This article will provide a concise description of the FV protein and gene and will review the molecular, clinical, and therapeutic aspects of FV deficiency.[ncbi.nlm.nih.gov] (congenital factor X deficiency) Stuart's D68.2 (congenital factor X deficiency) Dysfibrinogenemia D68.2 (congenital) Fibrinogenopenia D68.8 ICD-10-CM Diagnosis Code D68.8[icd10data.com]

  • Factor XII Deficiency

    (congenital factor X deficiency) Stuart's D68.2 (congenital factor X deficiency) Dysfibrinogenemia D68.2 (congenital) Fibrinogenopenia D68.8 ICD-10-CM Diagnosis Code D68.8[icd10data.com] Individuals affected by factor XII deficiency are primarily asymptomatic.[symptoma.com] Factor X Deficiency Also known as Stuart-Prower Factor Deficiency.[hemophiliawny.com]

  • Deficiency Disorder

    Kretschmer : The Stuart Prower Factor: Utilisation of Clotting Factors Obtained by Starch-Block Electrophoresis for Genetic Evaluation. Brit. J.[link.springer.com] This disease can be caused by malnutrition or an over dependence on a particular type of food or drink, such as maize or wine.[noorvitamins.com] Malnutrition can be prevented by getting adequate nutrition . Malnutrition tends to be more of a problem in developing countries.[medical-dictionary.thefreedictionary.com]

  • Hereditary Factor X Deficiency

    Hereditary factor X deficiency is an inherited coagulation disorder with an autosomal recessive transmission, resulting from a deficiency of factor X.[symptoma.com] Title Other Names: Factor X deficiency, congenital; Stuart factor deficiency, congenital; Stuart-Prower factor deficiency; Factor X deficiency, congenital; Stuart factor deficiency[rarediseases.info.nih.gov] A high-purity, plasma-derived FX concentrate (pdFX) has been developed for patients with hereditary FX deficiency.[ncbi.nlm.nih.gov]

  • Factor VII Deficiency

    Various preparations can be used in patients with FVII deficiency. Recombinant FVIIa is the optimal choice as a synthetic supply of the deficient clotting factor.[symptoma.com] (congenital factor X deficiency) Stuart's D68.2 (congenital factor X deficiency) Dysfibrinogenemia D68.2 (congenital) Fibrinogenopenia D68.8 ICD-10-CM Diagnosis Code D68.8[icd10data.com] This review describes the clinical picture of FVII deficiency and provides information on diagnosis and management of the disease.[ncbi.nlm.nih.gov]

  • Congenital Antithrombin III Deficiency

    Factor Stuart-Prower Deficiency XI Plasma Thromboplastin; Antecendent Hemophilia C XII Hageman Factor Not typically associated with bleeding XIII Fibrin Stabilizing Factor[rarebleedingdisorders.com] (Also known as/Synonyms) AT 3 Deficiency AT III Deficiency Hereditary Thrombophilia due to Antithrombin III Deficiency What is Antithrombin III Deficiency?[dovemed.com] Abstract Congenital antithrombin III (ATIII) deficiency, although uncommon, is a condition of considerable surgical importance.[ncbi.nlm.nih.gov]

  • Factor IX

    […] component [PTC] deficiency , F9 Deficiency , Deficiencies, F9 , Hemophilia B(M) , Plasma Thromboplastin Component Deficiency , Deficiency, F9 , F9 Deficiencies , Hemophilia[fpnotebook.com] Prower (FA10)* 105 2042 Factor XI (FA11)* 200 2527 Factor XII - Hageman (FA12)* 150 1877 Factor XIII - Fibrinaza (FA13)* 150 35 Fibrinogen 18 4607 Indice de protombina (IP[synlab.ro] Cranial hemophilic pseudotumors are extremely rare, with only 4 previous cases associated with mild or moderate factor XIII deficiency.[ncbi.nlm.nih.gov]

  • Congenital Afibrinogenemia

    Abstract A rare association of congenital afibrinogenemia and hereditary protein C deficiency is described in a 37-year-old female who suffered from ischemic necrosis in the[ncbi.nlm.nih.gov] (congenital factor X deficiency) (see also Defect, coagulation) 286.3 Stuart-Prower (congenital factor X deficiency) (see also Defect, coagulation) 286.3 Dysfibrinogenemia[icd9data.com] Rare coagulation factor deficiencies. In: Hoffman R, Benz EJ Jr, Silberstein LE, Heslop HE, Weitz JI, Anastasi J, eds.[m.ufhealth.org]

  • Hypofibrinogenemia

    Factor XIII (FXIII) deficiency is a rare bleeding disorder.[ingentaconnect.com] […] afibrinogenemia Deficiency of factor I [fibrinogen] Deficiency of factor II [prothrombin] Deficiency of factor V [labile] Deficiency of factor VII [stable] Deficiency of factor X [Stuart-Prower[icd10data.com] (congenital factor X deficiency) (see also Defect, coagulation) 286.3 Stuart-Prower (congenital factor X deficiency) (see also Defect, coagulation) 286.3 Dysfibrinogenemia[icd9data.com]

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