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115 Possible Causes for Anemia, patients possibly clinically asymptomatic, Variable Expressivity

Did you mean: Anemia, patients, possibly clinically asymptomatic, Variable Expressivity

  • Vitamin B12 Deficiency

    Anemia may make you feel tired, weak, and short of breath. What Causes Vitamin B12 Deficiency Anemia?[] Other newer areas of investigation that may provide better insights into the variability of expression of B 12 deficiency include genetic analysis and the effects of the microbiome[] A total of 62 asymptomatic vitamin B12 deficiency patients and 40 healthy subjects were included in the study and both groups were subjected to Standardized Mini-Mental State[]

  • Orthostatic Hypotension

    The case of a patient who developed aseptic meningitis, hemolytic anemia, hepatitis, and orthostatic hypotension simultaneously during treatment with trimethoprim-sulfamethoxazole[] We furthermore calculated within participant variability in SBP related to postural change, expressed as coefficient of variation.[] These findings suggest that clinically asymptomatic orthostatic hypotension in Parkinson's disease patients may acutely worsen neuropsychological performances with possible[]

  • Hypothyroidism

    Pernicious anemia, megaloblastic anemia (due to folic acid deficiency), some patients may present with leukopenia.[] Due to the rarity of the syndrome, the treatment strategies described are quite variable.[] Clinical Considerations Patient Population Under Consideration This recommendation applies to nonpregnant, asymptomatic adults.[]

  • Uterine Fibroid

    She does not remember being given a reason for anemia.[] In several studies, p53 had variable expression profiles when comparing leiomyosarcoma to leiomyoma variants.[] Summary of Recommended Treatment Options for Uterine Fibroids Patient characteristics Treatment options Asymptomatic women Clinical surveillance 4 Infertile women with distorted[]

  • Celiac Disease

    anemia.[] This cognitive involvement is variable in its expression, its duration and its prognosis ranging from transient and reversible subtle involvement to dementia itself.[] The clinical significance of possible low grade histologic inflammation in asymptomatic individuals is not known.[]

  • Juvenile Polyposis Syndrome

    In this study, we present an 8-month-old male infant of juvenile polyposis syndrome initially presenting with chronic anemia.[] Juvenile Polyposis has variable expressivity.[] Clinical management Genetic testing is advised for at-risk offspring of PJS patients when symptoms occur or in their late teens if they remain asymptomatic [ 6 ].[]

  • Inflammatory Bowel Disease Type 1

    Moreover, anemia may result from IBD therapies, such as sulfasalazine, which may confound the problem. 7 Anemia of inflammation or anemia of chronic disease (ACD) is characterized[] No outcome measures were expressed as continuous variables. Odds ratio, 95%CI, Forest and funnel plots were generated by Rev Man software.[] The best clinical approaches to PSC include colonoscopic examination with a biopsy to identify a possible asymptomatic UC and/or cancer and a prevention colonoscopy program[]

  • Sickle Cell Disease

    […] are no standard treatments that cure sickle cell anemia.[] Inflammation, haemolysis, microvascular obstruction and organ damage characterise the highly variable clinical expression of SCD.[] Asymptomatic cholelithiasis is common and should be followed clinically. Prophylactic cholecystectomy is generally not recommended.[]

  • Hereditary Elliptocytosis

    Auto-immune haemolytic anemia complicating infectious mononucleosis occurred in a patient with hereditary elliptocytosis.[] To define the cellular alteration(s) that best reflect the variable expression of the disease, we evaluated the pathobiologic features of red blood cells in a series of 18[] What features of the presentation will guide me toward possible causes and next treatment steps: The clinical presentation of HE is heterogenous, ranging from asymptomatic[]

  • Hypochromic Microcytic Anemia with Iron Overload Type 2

    This disease is a very rare severe non-syndromic hypochromic anemia, which is characterized by transfusion-dependent hypochromic, poorly regenerative anemia, iron overload[] The hereditary form is an X-linked recessive trait with variable expression.[] Clinical findings are variable and may be exacerbated by coinheritance of other genetic disorders and by parvovirus B19 infection. Most patients are asymptomatic.[]

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