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3,596 Possible Causes for Ectomorph, Iron Deficiency Anemia, Marfan Syndrome

  • Mitral Valve Prolapse

    KEYWORDS: Marfan syndrome; mitral valve prolapse[] Abstract Mitral valve prolapse (MVP) is a common pathological finding in several inherited connective-tissue diseases among which the Marfan syndrome.[] Abstract We describe the case of a 3-year-old child with neonatal Marfan syndrome complicated by mitral valve prolapse with regurgitation, marked aortic root dilatation, and[]

    Missing: Iron Deficiency Anemia
  • Duodenal Ulcer

    Seventy-nine percent of recurrences are asymptomatic with cirrhotic patients. 17 Patients of cirrhosis of liver can present with hematemesis, malena and iron deficiency anemia[]

    Missing: Marfan Syndrome
  • Marfan Syndrome

    Is there a test for Marfan syndrome? There is no single test for Marfan syndrome.[] Reviewed February 2008 What is Marfan syndrome? Marfan syndrome is a disorder of the connective tissue.[] The incidence of Marfan syndrome is approximately 1 in 5,000 worldwide. Mutations in the FBN1 gene cause Marfan syndrome .[]

    Missing: Iron Deficiency Anemia
  • Blue Sclera

    Other associations include: Ehler's danlos syndrome pseudoxanthoma elasticum Marfan's syndrome A blue sclera may also be acquired through long-term use of corticosteroids.[] Figure 1 Blue-tinged sclera secondary to severe iron deficiency anemia. Figure 1 Blue-tinged sclera secondary to severe iron deficiency anemia.[] These include osteogenesis imperfecta, Marfan's syndrome , Ehlers-Danlos syndrome , pseudoxanthoma elasticum , and Willems De Vries syndrome, among others.[]

    Missing: Ectomorph
  • Osteoporosis

    , Marfan syndrome , hemochromatosis , hypophosphatasia Other - Porphyria, sarcoid, immobilization, pregnancy/lactation, chronic obstructive pulmonary disease (COPD), parenteral[] Prevalence of occult celiac disease in patients with iron-deficiency anemia: a prospective study . South Med. J. 97 , 30–34 (2004). 26. Murray, J. A. et al .[] Genetic disorders - Marfan syndrome, osteogenesis imperfecta, hypophosphatasia, cystic fibrosis, glycogen storage diseases, hemochromatosis, and homocystinuria are examples[]

    Missing: Ectomorph
  • Connective Tissue Disease

    Marfan syndrome – a genetic disease causing abnormal fibrillin.[] Connective tissue diseases that are strictly due to genetic inheritance include Marfan syndrome (can have tissue abnormalities in the heart, aorta , lungs , eyes, and skeleton[] syndrome, Ehlers Danlos syndrome and osteogenesis imperfecta.[]

    Missing: Ectomorph Iron Deficiency Anemia
  • Heart Valve Disease

    It may be the result of connective tissue or immune disorders, such as Marfan syndrome or systemic lupus erythematosus, respectively.[] Diabetes and Marfan syndrome can also cause stenosis in the mitral valve.[] syndrome Symptoms of Heart Valve Disease Heart valve disease symptoms can vary depending on which valve is involved.[]

    Missing: Ectomorph
  • Factor VII Deficiency

    […] condition of Marfan syndrome, is extremely rare.[] Finally, iron deficiency anemia in women should be treated accordingly.[] Excluding two patients with severe, refractory menorrhagia ( 80 mL discharge/menses with profound iron-deficient anemia since the menarche, who were given a “personalized”[]

    Missing: Ectomorph
  • Hereditary Hemorrhagic Telangiectasia

    syndrome, Ehlers-Danlos syndrome, hereditary hemorrhagic telangiectasia) and especially specific characteristics of such diseases during pregnancy.[] Bevacizumab, a VEGF inhibitor, reduces epistaxis, telangiectasias, and iron-deficiency anemia.[] CONCLUSION: Arrhythmias are the most common cardiac phenotype in HHT, and likely to be aggravated by iron deficiency anemia, its treatments, and/or high output states due[]

    Missing: Ectomorph
  • Pneumothorax

    Also systemic connective tissue diseases such as rheumatic diseases and genetic syndroms like Marfan's syndrome can present with pneumothorax. idiopathic: often in young,[] […] presentations to primary care, the rates rise to 40.7 (men) and 15.6 (women) per 100 000 per year. 5 SP classically affects men more than women (ratio 2.5:1) 5 , 6 and those with ‘ectomorphic[] Genetic disorders that have been linked to PSP include Marfan syndrome , homocystinuria , and Birt-Hogg-Dube ( BHD ) syndrome.[]

    Missing: Iron Deficiency Anemia

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