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1,457 Possible Causes for Digitalis Toxicity, Fainting Spells, Mutation in the CALM2 Gene

  • Hypoglycemia

    We present a case of an 85-year-old man who presented to the endocrinology clinic with symptoms of "fainting spells after large meals."[ncbi.nlm.nih.gov] Because of the history of Billroth II surgery and the description of his fainting spells, a 5-hour glucose tolerance test was performed in the clinic using the foods that[ncbi.nlm.nih.gov]

    Missing: Mutation in the CALM2 Gene
  • Anemia

    INTRODUCTION Table 1 Etiopathogenic classification of anemia. Regenerative anemia Acute or chronic bleeding Hemolytic anemia Hereditary (hemoglobinopathy, enzymopathy, membrane-cytoskeletal defects) Acquired (autoimmune, mechanical destruction, toxic-metabolic, drugs, infectious, PNH, hypersplenism) Hypo-regenerative[…][dx.doi.org]

    Missing: Mutation in the CALM2 Gene
  • Cor Pulmonale

    Symptoms you may have are: Fainting spells during activity Chest discomfort, usually in the front of the chest Chest pain Swelling of the feet or ankles Symptoms of lung disorders[nlm.nih.gov] As the disease worsens, the following symptoms may occur with lighter activity, or even while you’re resting: 4 Fainting spells with activity Chest discomfort and/or chest[inogen.com]

    Missing: Mutation in the CALM2 Gene
  • Catecholaminergic Polymorphic Ventricular Tachycardia

    Possible complications include: Inability of the heart to pump enough blood (heart failure) Frequent fainting spells or unconsciousness Sudden death caused by cardiac arrest[mayoclinic.org] When ventricular fibrillation was induced electrically during digitalis toxicity, defibrillation could be accomplished readily but the toxic arrhythmia due to digitalis remained[scinapse.io] RYR2, CASQ2, KCNJ2 , ANK2, CALM1, CALM2, TRDN, SCN5A* Other Panels that Include this Diagnosis Notes on Genes: Priority Genes: These genes include 70% of the mutations that[admerahealth.com]

  • Acute Renal Failure

    Swiss Med Wkly. 2012 Aug 14;142:w13662. doi: 10.4414/smw.2012.13662. eCollection 2012. Author information 1 Pediatric Cardiac Anesthesia/Intensive Care Unit, Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital, Rome, Italy. accaria.ricci@gmail.com Abstract The term acute kidney injury (AKI)[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the CALM2 Gene
  • Catecholaminergic Polymorphic Ventricular Tachycardia Type 2

    toxicity.[ncbi.nlm.nih.gov] For individuals who have problems with chronic fainting spells, therapy should focus on recognizing the triggers and learning techniques to keep from fainting.[en.wikipedia.org] […] that have been discovered and only represent a small percentage of CPVT cases are TRDN (encoding triadin) and CALM1 (encoding calmodulin). 5,6 Mutations in the CALM2 gene[doi.org]

  • Hypokalemia

    Susceptibility to digitalis toxicity is increased when a patient has hypokalemia.[medical-dictionary.thefreedictionary.com] toxicity non-steroidal anti-inflammatory drugs: reduced diuretic efficacy beta-blockers: potentiate hyperglycemia, hyperlipidemias corticosteroids: enhance hypokalemia Loop[cvpharmacology.com] toxicity non-steroidal anti-inflammatory drugs: reduced diuretic efficacy corticosteroids: enhance hypokalemia aminoglycosides: enhance ototoxicity, nephrotoxicity K -sparing[cvpharmacology.com]

    Missing: Mutation in the CALM2 Gene
  • Conn Syndrome

    Article Navigation 1 Departments of Medicine (S.-C.T., C.-H.C., Y.-W.N., F.W.K.C., C.-M.N., A.P.S.K.)Hong Kong Special Administrative Region, China * Address all correspondence and requests for reprints to: Sau-Cheung Tiu, Department of Medicine, Queen Elizabeth Hospital, 30 Gascoigne Road, Hong Kong Special Administrative[…][doi.org]

    Missing: Mutation in the CALM2 Gene
  • Insulinoma

    Insulinoma associated with pregnancy is a very rare condition and can be difficult to diagnose. Here, we present an interesting case of insulinoma occurring during pregnancy with special attention paid to the use of a continuous glucose monitoring system to detect hypoglycemia. A 36-year-old white woman in the[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the CALM2 Gene
  • Hypernatremia

    Hypernatremia is a frequent occurrence among hospitalized patients. Severe hypernatremia is associated with mortality rates of over 60 %. Extreme hypernatremia, defined as sodium levels 190 mmol/l, is a rare occurrence. The literature on electrocardiographic changes occurring with this degree of hypernatremia is[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the CALM2 Gene