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Disease Information for Vitamin E deficiency
- Clinical Manifestations
- Signs & Symptoms
- Edema Children
- Malnourished/poor nutrition status/signs
- Edema of Lower Extremities
- Muscle weakness
- Absent deep tendon reflexes
- Absent knee reflexes
- Ankle reflexes absent
- Ataxia
- Awkward Uncoordinated Child
- Cerebellar movement disorder/signs
- Cerebellar signs
- Dysarthria
- Dysdiadochokinesia/Alternating failure
- Hyporeflexia/DTRs decreased
- Lhermittes sign (tingling on neck flex)
- Limb Ataxia
- Limb ataxia/clumsiness child
- Loss position sense/postural sense
- Neurologic manifestations/signs
- Position sense decreased/proprioception
- Position sense decreased/proprioception Legs
- Sensory defects/lower extremities
- Slurred speech
- Slurred Speech/Acute
- Slurred speech/Chronic
- Staggering Gait
- Truncal ataxia
- Unable to tandem walk/straight line
- Vibratory sense decreased
- Vibratory sense decreased Legs
- Difficulty Talking
- Walking difficulties
- Weakness
- Double Image Vision Confirmed
- Eyelid Retraction
- Proptosis,bilateral
- Ptosis (blepharoptosis)
- Retinal pigmentation
- Clinical Presentation & Variations
- Anemia in Children
- Presentation/Ataxia in a Child Acute
- Demographics & Risk Factors
- Established Disease Population
- Patient/Malnourished/starved
- Patient/Malabsorption syndrome
- Laboratory Tests
- Microbiology & Serology Findings
- Reticulocytosis
- Abnormal Lab Findings - Decreased
- Factor 2/Prothrombin (Lab)
- Hemoglobin (Lab)
- Abnormal Lab Findings - Increased
- CPK/CK/Creatine kinase/Creatine phosphokinase (Lab)
- Polychrome RBCs (Lab)
- Reticulocytes (Lab)
- URINE Creatine
- URINE Hemoglobin
- Diagnostic Test Results
- Pathology
- BX/Muscle Biopsy Abnormal
- BX/Muscle biopsy/Ceroid deposition
- Associated Diseases & Rule outs
- Rule Outs
- Ataxia-telangiectasia
- Friedreich's Ataxia
- Tabes dorsalis
- Associated Disease & Complications
- Carcinomatous cerebellar/motor syndrome
- Cerebellar ataxia
- Edema
- Exophthalmos
- Hemoglobinuria
- Hemolysis anemia/acute/active
- Hereditary Blindness
- Myelopathy manifestations/involvement
- Ophthalmoplegia
- Peripheral neuropathy
- Polyneuritis
- Retinal Degeneration/Dystrophy
- Retinitis pigmentosa
- Vitamin E deficiency
- Ataxia Disorder
- Polyneuropathy
- Disease Synergy - Causes
- Synergy/Malabsorption syndrome
- Disease Mechanism & Classification
- Pathophysiology
- Pathophysiology/Hemolytic process/effect
- Pathophysiology/Acquired Neuropathy
- Pathophysiology/Posterior columns cord def
- Process
- PROCESS/Deficiency (category)
- Synonyms
- Synonym
- DEFIC VITAMIN E, Deficiencies Vitamin E, Deficiency of vitamin E, deficiency vitamin E, Hypovitaminosis E, vitamin deficiency E, VITAMIN E DEFIC, Vitamin E Deficiencies, Vitamin E deficiency, Vitamin E deficiency (disorder), Vitamin E deficiency disease, Early Onset Ataxia/Children
- Treatment
- Drug Therapy - Indication
- RX/Vitamin E
- Definition
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A nutritional condition produced by a deficiency of VITAMIN E in the diet, characterized by posterior column and spinocerebellar tract abnormalities, areflexia, ophthalmoplegia, and disturbances of gait, proprioception, and vibration; In premature infants vitamin E deficiency is associated with hemolytic anemia, thrombocytosis, edema, intraventricular hemorrhage, and increasing risk of retrolental fibroplasia and bronchopulmonary dysplasia; An apparent inborn error of vitamin E metabolism, named familial isolated vitamin E deficiency, has recently been identified. (Cecil Textbook of Medicine, 19th ed,)-----------------------.
In general, tocopherols act as antioxidants to prevent lipid peroxidation of polyunsaturated fatty acids in cellular membranes; The antioxidant activity of -tocopherol is similar to that of glutathione peroxidase, which contains selenium; the main manifestations of vitamin E deficiency are (1) mild hemolytic anemia associated with increased erythrocyte hemolysis and (2) spinocerebellar disease , which occurs mainly in children who have fat malabsorption due to abetalipoproteinemia, chronic cholestatic hepatobiliary disease, celiac disease, or a genetic abnormality in vitamin E metabolism; Retinopathy of prematurity, also called retrolental fibroplasia, may improve with vitamin E therapy, and hemorrhage in the newborn; Infants are born in a state of relative vitamin E deficiency, with plasma -tocopherol levels below 5 µg/mL; The smaller and more premature the infant, the greater the degree of deficiency; Vitamin E deficiency in premature infants persists during the first few weeks of life and can be attributed to limited placental transfer of vitamin E, low tissue levels at birth, relative dietary deficiency in infancy, intestinal malabsorption, and rapid growth; As the digestive system matures, vitamin E absorption improves, and blood vitamin E levels rise; malabsorption generally underlies vitamin E deficiency; Genetic abnormality in the transport of vitamin E can also play a role; Hemolytic anemia in premature infants may be a manifestation of vitamin E deficiency; Such an infant has hemoglobin levels ranging from 7 to 9 g/dL, low plasma vitamin E levels, reticulocytosis, and hyperbilirubinemia;
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- External Links Related to Vitamin E deficiency
- Wikipedia
- Merck
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- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)