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The anemia in multiple myeloma is normocytic normochromic (normal mean corpuscular volume "MCV").
Neurological symptoms include neuropathy as well as radiculopathy.
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G6PD deficiency (favism) is an x-linked recessive disorder, therefore more common in males than females.
G6PD deficiency is protective against Plasmodium falciparum malaria.
Patients may experience an acute hemolytic episode after consuming fava beans (that's why it's called "favism"). Fave beans, in this case, is an oxidative agent.
Symptoms include jaundice (yellow skin, dark urine), fatigue, pallor, drowsiness, exercise intolerance, shortness of breath, abdominal, or lumbar pain.
The most common stressor in G6PD deficiency is infections.
Reticulocyte count will be high in this case
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Glanzmann Thrombasthenia (GT) is an autosomal recessive defect in the GPIIb/IIIa (GP2b/3a) receptor on the platelet which leads to defective platelet aggregation.
Bernard-Soulier Syndrome (BSS) is an autosomal recessive (AR) disorder characterized by a defective GP1b platelet receptor leading to a problematic platelet adhesion process (primary hemostasis).
Ristocetin Cofactor Assay (RIPA) is usually abnormal in cases of Bernard-Soulier Syndrome (BSS).
Bleeding time is prolonged, platelets are big in size, but few in number (Macrothrombocytopenia).
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Platelet count is one of the lab tests used by a doctor or a hematologist to assess whether your platelet number is normal, low (thrombocytopenia) or high (thrombocytosis).
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