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111 Possible Causes for Coagulation Factor Disorder, Microcytic Anemia, Nail Abnormality

  • Anemia

    VIII deficiency D67 Hereditary factor IX deficiency D68 Other coagulation defects D68.0 Von Willebrand's disease D68.1 Hereditary factor XI deficiency D68.2 Hereditary deficiency[icd10data.com] The anemia is then categorized as microcytic, macrocytic or normocytic, with or without reticulocytosis.[ncbi.nlm.nih.gov] FFP and cryoprecipitate can be used to correct coagulation factor and fibrinogen deficiency.[emedicine.com]

  • Normocytic Normochromic Anemia

    VIII deficiency D67 Hereditary factor IX deficiency D68 Other coagulation defects D68.0 Von Willebrand's disease D68.1 Hereditary factor XI deficiency D68.2 Hereditary deficiency[icd10data.com] anemia- iron deficiency, anemia of chronic disease, thalassemia minor, sideroblastic anemia Microcytic anemia 1.[slideshare.net] Hypochromic microcytic anemias include: Iron deficiency anemia: The most common cause of microcytic anemia is an iron deficiency in the blood.[healthline.com]

  • Hereditary Sideroblastic Anemia

    […] deficiency of other clotting factors D6831Hemorrhagic disorder due to intrinsic circulating anticoagulants D6832Hemorrhagic disorder due to extrinsic circulating anticoagulants[cms.gov] Hypochromic microcytic anemias include: Iron deficiency anemia: The most common cause of microcytic anemia is an iron deficiency in the blood.[healthline.com] 慢性骨髄増殖性疾患 coagulation factor凝固因子 complete remission (CR)完全寛解 concentrated red cells濃厚赤血球 consolidation therapy地固め療法 cord blood stem cell transplantation (CBT)臍帯血移植 d dendritic[tokyo-med.ac.jp]

  • Liver Cirrhosis

    factors and disorders of fibrinolysis.[ncbi.nlm.nih.gov] (low hematocrit, hemoglobin and microcytic anemia), High polynuclear leukocytes, and thrombocytes (on a Complete Blood Count of the White Blood Cells [WBC's]), and many other[autoinflammatory.org] Prothrombin time (PT) is elevated due to coagulation factor defects as well as bilirubin, while albumin is low as it is synthesized by the liver and the liver's functional[ncbi.nlm.nih.gov]

  • Vitamin Deficiency

    Chronic toxicity causes changes in skin, hair, and nails; abnormal liver test results; and, in a fetus, birth defects. Diagnosis is usually clinical.[merckmanuals.com] Inherited combined deficiency of the vitamin K-dependent clotting factors (VKCFD) is a very rare inherited bleeding disorder that is caused by a problem with clotting factors[wfh.org] Signs and symptoms include microcytic anemia, electroencephalographic abnormalities, dermatitis, depression and confusion.[en.wikipedia.org]

  • Celiac Disease

    At the same time, however, patients can experience a loss of sensation, and inability to feel painful stimuli, as when stepping on a sharp nail or burning the fingers on a[web.archive.org] A decrease in K vitamin–dependent coagulation factors results in prolongation of coagulation assays such as the prothrombin time (PT), international normalized ratio (INR)[bloodjournal.org] Symptoms of autonomic small fiber neuropathy include abnormal sweating or temperature regulation, lightheadedness or fainting when standing up from hypotension or tachycardia[web.archive.org]

  • Hypermenorrhea

    Note any signs suggestive of endocrine abnormality (hirsutism, acne) or bruising. Look at the tongue for pallor and the nails for koilonychia.[patient.info] Other coagulation factor deficiencies, hemophilia, and platelet function disorders may be associated with AUB in any age group.[acog.org] Some blood coagulation disorders — such as von Willebrand’s disease, a condition in which an important blood-clotting factor is deficient or impaired — can cause abnormal[pharmacypedia.org]

  • Normochromic Anemia

    Nail dystrophy Mucosal leukoplakia Non-cutaneous abnormalities dental, genitourinary, gastrointestinal, neurological ophthalmic, pulmonary & skeletal 80%:Males(X-linked form[authorstream.com] VIII deficiency D67 Hereditary factor IX deficiency D68 Other coagulation defects D68.0 Von Willebrand's disease D68.1 Hereditary factor XI deficiency D68.2 Hereditary deficiency[icd10data.com] A renal-cell carcinoma was discovered and resected in a 38-year-old female patient who had microcytic normochromic anemia.[academic.oup.com]

  • Sickle Cell Disease

    Keywords: sickle cell, hemolysis, coagulation, tissue factor, inflammation Introduction Sickle cell anemia is the most common and severe variant of sickle cell disease.[ncbi.nlm.nih.gov] Some causes of microcytic anemia, most notably iron deficiency, are characterized by an increase in RDW.[web.archive.org] Patients with Hb SS and Hb SC have a normocytic anemia, unless they have coinherited α-thalassemia. Patients with Hb Sβ and Hb Sβ 0 have a microcytic anemia. Table II.[clinicaladvisor.com]

  • FLOTCH Syndrome

    Evaluation of nail abnormalities. Am Fam Physician. 2012;85:779–87. PubMed Google Scholar 8. Moreno-Coutino G, Toussaint-Caire S, Arenas R.[link.springer.com] Deficiency of this factor affects clot stability, FXIIID, while generally rare, does occur, with Iran having the highest global incidence of the disorder with 473 cases.[wikivisually.com] , Megalocytic-normochromic anemia, Menorrhagia, Methyldopa-induced immune hemolytic anemia, Microcytic anemia, Microcytic hyperchromic anemia, Microcytic hypochromic anemia[wikidoc.org]

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