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52 Possible Causes for Benign Asymptomatic Defect

  • Bradyarrhythmia

    […] congenital defects of the vessels, chambers, or valves of the heart.[en.wikipedia.org] Among the many alternative causes are episodes of isolated arrhythmias which degenerated into lethal VF and asystole, and various unnoticed, possibly asymptomatic cardiac[en.wikipedia.org] If sudden cardiac death occurs, it is usually because of pathological hypertrophic enlargement of the heart that went undetected or was incorrectly attributed to the benign[en.wikipedia.org]

  • Arterial Embolism

    Received September 29, 2016 Received in revised form December 20, 2016 Accepted December 23, 2016 1 Introduction EA is a benign and stable congenital heart disease for asymptomatic[journals.lww.com] When combined atrial septal defect, patent foramen ovale, arterial embolism and other reasons are all excluded, it is often considered to be the consequence of paradoxical[journals.lww.com]

  • Juvenile Rheumatoid Arthritis

    Pulmonary disease in JIA is usually a benign, extra-articular manifestation, characterised mainly by asymptomatic defects of pulmonary function, pleuritis, or pneumonitis.[ard.bmj.com]

  • Bone Tumor

    One of the most common benign lytic lesions seen Asymptomatic and usually an incidental finding Most often seen around the knee and distal tibia Non-Ossifying fibroma generally[imageinterpretation.co.uk] […] bigger than 2cm Fibrous Cortical Defect generally smaller than 2cm Arises in the under 30 year age group Develops from cortex of metaphysis; is eccentric within the bone[imageinterpretation.co.uk] […] time to consolidate Soft tissue involvement Aggressive lesions often lead to cortical breakthrough to create a soft tissue mass Non-Ossifying Fibroma / Fibrous Cortical Defect[imageinterpretation.co.uk]

  • Malignant Bone Neoplasm

    One of the most common benign lytic lesions seen Asymptomatic and usually an incidental finding Most often seen around the knee and distal tibia Non-Ossifying fibroma generally[imageinterpretation.co.uk] […] bigger than 2cm Fibrous Cortical Defect generally smaller than 2cm Arises in the under 30 year age group Develops from cortex of metaphysis; is eccentric within the bone[imageinterpretation.co.uk] […] time to consolidate Soft tissue involvement Aggressive lesions often lead to cortical breakthrough to create a soft tissue mass Non-Ossifying Fibroma / Fibrous Cortical Defect[imageinterpretation.co.uk]

  • Hemangioma

    DISCUSSION Presentation Calvarial hemangiomas are benign, malformed vascular lesions, are usually asymptomatic, and are usually discovered incidentally on imaging or postmortem[surgicalneurologyint.com] […] sagittal and bone window) image showing the hypodense lesions in parietal region Figure 5 Postoperative X-ray skull anteroposterior and lateral view showing postoperative defect[surgicalneurologyint.com]

  • Kostmann Syndrome

    It is associated with a gene defect termed ELA2. A third form, benign chronic neutropenia, has low, but not life threatening, neutropenia and is often asymptomatic.[primaryimmune.org]

  • Hereditary Hyperekplexia

    […] syndrome Short-sleeper Familial benign hypercalcemia Familial hypocalciuric hypercalcemia (FHH) is a generally asymptomatic genetic disorder of phosphocalcic metabolism characterized[amp.pharm.mssm.edu] Ventricular septal defect 3 Ventricular septal defect 1 Epilepsy, progressive myoclonic 4, with or without renal failure Cystinosis Knuckle pads, deafness AND leukonychia[amp.pharm.mssm.edu] Common variable immunodeficiency 8, with autoimmunity Angiotensin i-converting enzyme, benign serum increase Fleck corneal dystrophy Fleck corneal dystrophy (FCD) is a rare[amp.pharm.mssm.edu]

  • Transient Familial Neonatal Hyperbilirubinemia

    DJS in a benign disease, and in adolescents and adults, it does not require treatment.[nature.com] Increased severity in neonates has been attributed to immature bile physiology combined with the MRP2 defect.[nature.com] As the liver matures, infants become asymptomatic until later in life, when they can present with intermittent hyperbilirubinemia ( 74 ). Diagnosis and management.[nature.com]

  • Disorder of Fructose Metabolism

    Due to defect in FRUCTOKINASE. Autosomal recessive. Benign, asymptomatic.[quizlet.com]

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